Canonical Allele Identifier: CA1963577569
Community Standard Title: NM_000610.4(CD44):c.1436T= (p.Ile479=)
Gene: CD44 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.35208126T= , CM000673.2:g.35208126T= GRCh38
NC_000011.9:g.35229673T= , CM000673.1:g.35229673T= GRCh37
NC_000011.8:g.35186249T= NCBI36
NG_008937.1:g.74257T=

Transcript Alleles

HGVS Amino-acid Change
NM_000610.4:c.1436T= MANE Select NP_000601.3:p.Ile479=
ENST00000428726.8:c.1436T= MANE Select ENSP00000398632.2:p.Ile479=
NM_000610.3:c.1436T= NP_000601.3:p.Ile479=
NM_001001389.1:c.1307T= NP_001001389.1:p.Ile436=
NM_001001389.2:c.1307T= NP_001001389.1:p.Ile436=
NM_001001390.1:c.689T= NP_001001390.1:p.Ile230=
NM_001001390.2:c.689T= NP_001001390.1:p.Ile230=
NM_001001391.1:c.668-6726T= NP_001001391.1:n.668-6726T=
NM_001001391.2:c.668-6726T= NP_001001391.1:n.668-6726T=
NM_001001392.1:c.234-13579T= NP_001001392.1:n.234-13579T=
NM_001001392.2:c.234-13579T= NP_001001392.1:n.234-13579T=
NM_001202555.1:c.668-3120T= NP_001189484.1:n.668-3120T=
NM_001202555.2:c.668-3120T= NP_001189484.1:n.668-3120T=
NM_001202556.1:c.668-11190T= NP_001189485.1:n.668-11190T=
NM_001202556.2:c.668-11190T= NP_001189485.1:n.668-11190T=
NM_001202557.1:c.668-6726T= NP_001189486.1:n.668-6726T=
NM_001202557.2:c.668-6726T= NP_001189486.1:n.668-6726T=
ENST00000263398.10:c.668-6726T= ENSP00000263398.6:n.668-6726T=
ENST00000263398.11:c.668-6726T= ENSP00000263398.6:n.668-6726T=
ENST00000278385.10:c.197T= ENSP00000278385.6:p.Ile66=
ENST00000278386.10:c.234-13579T= ENSP00000278386.6:n.234-13579T=
ENST00000279452.10:c.455-6726T= ENSP00000279452.6:n.455-6726T=
ENST00000352818.8:c.668-11190T= ENSP00000309732.6:n.668-11190T=
ENST00000415148.6:c.1307T= ENSP00000389830.2:p.Ile436=
ENST00000425428.6:c.*291-6726T= ENSP00000395953.2:n.*291-6726T=
ENST00000428726.6:c.1436T= ENSP00000398632.2:p.Ile479=
ENST00000433892.6:c.689T= ENSP00000392331.2:p.Ile230=
ENST00000434472.6:c.668-3120T= ENSP00000404447.2:n.668-3120T=
ENST00000442151.6:c.666-6726T=
ENST00000525211.6:c.821T= ENSP00000432405.2:p.Ile274=
ENST00000525293.5:n.168-3120T=
ENST00000525685.5:c.547T=
ENST00000525685.6:c.547T=
ENST00000525688.5:c.311-6726T= ENSP00000436980.1:n.311-6726T=
ENST00000526000.5:c.509-3120T= ENSP00000434465.1:n.509-3120T=
ENST00000526000.6:c.508-3120T=
ENST00000526553.5:c.393T=
ENST00000526553.6:c.393T=
ENST00000526669.6:c.290-11214T= ENSP00000432704.2:n.290-11214T=
ENST00000527889.5:c.463T=
ENST00000527889.6:c.463T=
ENST00000528086.5:n.501-11T=
ENST00000528672.1:c.260T= ENSP00000431860.1:p.Ile87=
ENST00000531110.5:c.572T= ENSP00000436549.1:p.Ile191=
ENST00000531110.6:c.572T= ENSP00000436549.2:p.Ile191=
ENST00000531873.5:c.430-1839T=
ENST00000532339.1:n.551T=
ENST00000533222.5:c.314T= ENSP00000435321.1:p.Ile105=
ENST00000639002.1:c.59-60T= ENSP00000492449.1:n.59-60T=
XM_005253231.2:c.1439T= XP_005253288.1:p.Ile480=
XM_005253231.3:c.1439T= XP_005253288.1:p.Ile480=
XM_005253232.2:c.1436T= XP_005253289.1:p.Ile479=
XM_005253232.3:c.1436T= XP_005253289.1:p.Ile479=
XM_005253233.2:c.1319T= XP_005253290.1:p.Ile440=
XM_005253234.2:c.1316T= XP_005253291.1:p.Ile439=
XM_005253235.2:c.1310T= XP_005253292.1:p.Ile437=
XM_005253235.3:c.1310T= XP_005253292.1:p.Ile437=
XM_005253238.2:c.950T= XP_005253295.1:p.Ile317=
XM_005253238.3:c.950T= XP_005253295.1:p.Ile317=
XM_005253239.2:c.944T= XP_005253296.1:p.Ile315=
XM_005253239.3:c.944T= XP_005253296.1:p.Ile315=
XM_005253240.2:c.815T= XP_005253297.1:p.Ile272=
XM_005253240.3:c.815T= XP_005253297.1:p.Ile272=
XM_006718388.1:c.1433T= XP_006718451.1:p.Ile478=
XM_006718388.2:c.1433T= XP_006718451.1:p.Ile478=
XM_011520482.1:c.1439T= XP_011518784.1:p.Ile480=
XM_011520482.2:c.1439T= XP_011518784.1:p.Ile480=
XM_011520483.1:c.1184T= XP_011518785.1:p.Ile395=
XM_011520483.2:c.1184T= XP_011518785.1:p.Ile395=
XM_011520484.1:c.1181T= XP_011518786.1:p.Ile394=
XM_011520484.2:c.1181T= XP_011518786.1:p.Ile394=
XM_011520485.1:c.1178T= XP_011518787.1:p.Ile393=
XM_011520485.2:c.1178T= XP_011518787.1:p.Ile393=
XM_011520486.1:c.821T= XP_011518788.1:p.Ile274=
XM_011520486.2:c.821T= XP_011518788.1:p.Ile274=
XM_011520488.1:c.689T= XP_011518790.1:p.Ile230=
XM_011520488.2:c.689T= XP_011518790.1:p.Ile230=
XM_017018583.2:c.1307T= XP_016874072.1:p.Ile436=
XM_017018584.2:c.923-6726T= XP_016874073.1:n.923-6726T=
XM_017018585.2:c.794-6726T= XP_016874074.1:n.794-6726T=