Canonical Allele Identifier: CA13503701
Gene: CD44 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.35228123A>G , CM000673.2:g.35228123A>G GRCh38
NC_000011.9:g.35249670A>G , CM000673.1:g.35249670A>G GRCh37
NC_000011.8:g.35206246A>G NCBI36
NG_008937.1:g.94254A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263398.11:c.882-1006A>G ENSP00000263398.6:n.882-1006A>G
ENST00000428726.8:c.2025-1006A>G MANE Select ENSP00000398632.2:n.2025-1006A>G
ENST00000263398.10:c.882-1006A>G ENSP00000263398.6:n.882-1006A>G
ENST00000278385.10:c.582-1006A>G ENSP00000278385.6:n.582-1006A>G
ENST00000278386.10:c.262-1006A>G ENSP00000278386.6:n.262-1006A>G
ENST00000279452.10:c.669-1006A>G ENSP00000279452.6:n.669-1006A>G
ENST00000352818.8:c.819-1006A>G ENSP00000309732.6:n.819-1006A>G
ENST00000415148.6:c.1896-1006A>G ENSP00000389830.2:n.1896-1006A>G
ENST00000425428.6:c.*505-1006A>G ENSP00000395953.2:n.*505-1006A>G
ENST00000428726.6:c.2025-1006A>G ENSP00000398632.2:n.2025-1006A>G
ENST00000433892.6:c.1278-1006A>G ENSP00000392331.2:n.1278-1006A>G
ENST00000434472.6:c.1086-1006A>G ENSP00000404447.2:n.1086-1006A>G
ENST00000525469.1:c.45-1006A>G ENSP00000434920.1:n.45-1006A>G
ENST00000525688.5:c.525-1006A>G ENSP00000436980.1:n.525-1006A>G
ENST00000526669.6:c.417-1006A>G ENSP00000432704.2:n.417-1006A>G
ENST00000527326.1:n.401-1006A>G
NM_000610.3:c.2025-1006A>G NP_000601.3:n.2025-1006A>G
NM_001001389.1:c.1896-1006A>G NP_001001389.1:n.1896-1006A>G
NM_001001390.1:c.1278-1006A>G NP_001001390.1:n.1278-1006A>G
NM_001001391.1:c.882-1006A>G NP_001001391.1:n.882-1006A>G
NM_001001392.1:c.262-1006A>G NP_001001392.1:n.262-1006A>G
NM_001202555.1:c.1086-1006A>G NP_001189484.1:n.1086-1006A>G
NM_001202556.1:c.819-1006A>G NP_001189485.1:n.819-1006A>G
XM_005253231.2:c.2028-1006A>G XP_005253288.1:n.2028-1006A>G
XM_005253232.2:c.2025-1006A>G XP_005253289.1:n.2025-1006A>G
XM_005253233.2:c.1908-1006A>G XP_005253290.1:n.1908-1006A>G
XM_005253234.2:c.1905-1006A>G XP_005253291.1:n.1905-1006A>G
XM_005253235.2:c.1899-1006A>G XP_005253292.1:n.1899-1006A>G
XM_005253238.2:c.1539-1006A>G XP_005253295.1:n.1539-1006A>G
XM_005253239.2:c.1533-1006A>G XP_005253296.1:n.1533-1006A>G
XM_005253240.2:c.1404-1006A>G XP_005253297.1:n.1404-1006A>G
XM_006718388.1:c.2022-1006A>G XP_006718451.1:n.2022-1006A>G
XM_011520482.1:c.1824-1006A>G XP_011518784.1:n.1824-1006A>G
XM_011520483.1:c.1773-1006A>G XP_011518785.1:n.1773-1006A>G
XM_011520484.1:c.1770-1006A>G XP_011518786.1:n.1770-1006A>G
XM_011520485.1:c.1767-1006A>G XP_011518787.1:n.1767-1006A>G
XM_011520486.1:c.1410-1006A>G XP_011518788.1:n.1410-1006A>G
XM_011520488.1:c.1074-1006A>G XP_011518790.1:n.1074-1006A>G
XM_005253231.3:c.2028-1006A>G XP_005253288.1:n.2028-1006A>G
XM_005253232.3:c.2025-1006A>G XP_005253289.1:n.2025-1006A>G
XM_005253235.3:c.1899-1006A>G XP_005253292.1:n.1899-1006A>G
XM_005253238.3:c.1539-1006A>G XP_005253295.1:n.1539-1006A>G
XM_005253239.3:c.1533-1006A>G XP_005253296.1:n.1533-1006A>G
XM_005253240.3:c.1404-1006A>G XP_005253297.1:n.1404-1006A>G
XM_006718388.2:c.2022-1006A>G XP_006718451.1:n.2022-1006A>G
XM_011520482.2:c.1824-1006A>G XP_011518784.1:n.1824-1006A>G
XM_011520483.2:c.1773-1006A>G XP_011518785.1:n.1773-1006A>G
XM_011520484.2:c.1770-1006A>G XP_011518786.1:n.1770-1006A>G
XM_011520485.2:c.1767-1006A>G XP_011518787.1:n.1767-1006A>G
XM_011520486.2:c.1410-1006A>G XP_011518788.1:n.1410-1006A>G
XM_011520488.2:c.1074-1006A>G XP_011518790.1:n.1074-1006A>G
XM_017018583.2:c.1896-1006A>G XP_016874072.1:n.1896-1006A>G
XM_017018584.2:c.1137-1006A>G XP_016874073.1:n.1137-1006A>G
XM_017018585.2:c.1008-1006A>G XP_016874074.1:n.1008-1006A>G
NM_000610.4:c.2025-1006A>G MANE Select NP_000601.3:n.2025-1006A>G
NM_001001389.2:c.1896-1006A>G NP_001001389.1:n.1896-1006A>G
NM_001001390.2:c.1278-1006A>G NP_001001390.1:n.1278-1006A>G
NM_001001391.2:c.882-1006A>G NP_001001391.1:n.882-1006A>G
NM_001001392.2:c.262-1006A>G NP_001001392.1:n.262-1006A>G
NM_001202555.2:c.1086-1006A>G NP_001189484.1:n.1086-1006A>G
NM_001202556.2:c.819-1006A>G NP_001189485.1:n.819-1006A>G
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