Canonical Allele Identifier: CA4293124

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.74060154G>A , CM000669.2:g.74060154G>A GRCh38
NC_000007.13:g.73474484G>A , CM000669.1:g.73474484G>A GRCh37
NC_000007.12:g.73112420G>A NCBI36
NG_009261.1:g.37058G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000692049.1:c.1678G>A (ELN) ENSP00000510104.1:p.Ala560Thr
ENST00000252034.12:c.1591G>A (ELN) MANE Select ENSP00000252034.7:p.Ala531Thr
ENST00000252034.11:c.1591G>A (ELN) ENSP00000252034.7:p.Ala531Thr
ENST00000320399.10:c.1591G>A (ELN) ENSP00000313565.6:p.Ala531Thr
ENST00000320492.11:c.1348G>A (ELN) ENSP00000315607.7:p.Ala450Thr
ENST00000357036.9:c.1606G>A (ELN) ENSP00000349540.5:p.Ala536Thr
ENST00000358929.8:c.1678G>A (ELN) ENSP00000351807.5:p.Ala560Thr
ENST00000380553.8:c.1183G>A (ELN) ENSP00000369926.4:p.Ala395Thr
ENST00000380562.8:c.1609G>A (ELN) ENSP00000369936.4:p.Ala537Thr
ENST00000380575.8:c.1504G>A (ELN) ENSP00000369949.4:p.Ala502Thr
ENST00000380576.9:c.1534G>A (ELN) ENSP00000369950.5:p.Ala512Thr
ENST00000380584.8:c.1477+107G>A (ELN) ENSP00000369958.4:n.1477+107G>A
ENST00000414324.5:c.1519G>A (ELN) ENSP00000392575.1:p.Ala507Thr
ENST00000429192.5:c.1549G>A (ELN) ENSP00000391129.1:p.Ala517Thr
ENST00000445912.5:c.1591G>A (ELN) ENSP00000389857.1:p.Ala531Thr
ENST00000458204.5:c.1561G>A (ELN) ENSP00000403162.1:p.Ala521Thr
ENST00000621115.4:c.1324G>A (ELN) ENSP00000480955.1:p.Ala442Thr
NM_000501.3:c.1591G>A (ELN) NP_000492.2:p.Ala531Thr
NM_001081752.2:c.1504G>A (ELN) NP_001075221.1:p.Ala502Thr
NM_001081753.2:c.1549G>A (ELN) NP_001075222.1:p.Ala517Thr
NM_001081754.2:c.1606G>A (ELN) NP_001075223.1:p.Ala536Thr
NM_001081755.2:c.1534G>A (ELN) NP_001075224.1:p.Ala512Thr
NM_001278912.1:c.1591G>A (ELN) NP_001265841.1:p.Ala531Thr
NM_001278913.1:c.1348G>A (ELN) NP_001265842.1:p.Ala450Thr
NM_001278914.1:c.1519G>A (ELN) NP_001265843.1:p.Ala507Thr
NM_001278915.1:c.1609G>A (ELN) NP_001265844.1:p.Ala537Thr
NM_001278916.1:c.1477+107G>A (ELN) NP_001265845.1:n.1477+107G>A
NM_001278917.1:c.1561G>A (ELN) NP_001265846.1:p.Ala521Thr
NM_001278918.1:c.1324G>A (ELN) NP_001265847.1:p.Ala442Thr
NM_001278939.1:c.1678G>A (ELN) NP_001265868.1:p.Ala560Thr
XM_005250187.1:c.1555G>A (ELN) XP_005250244.1:p.Ala519Thr
XM_005250188.1:c.1549G>A (ELN) XP_005250245.1:p.Ala517Thr
XM_011515868.1:c.1606G>A (ELN) XP_011514170.1:p.Ala536Thr
XM_011515869.1:c.1576G>A (ELN) XP_011514171.1:p.Ala526Thr
XM_011515870.1:c.1570G>A (ELN) XP_011514172.1:p.Ala524Thr
XM_011515871.1:c.1564G>A (ELN) XP_011514173.1:p.Ala522Thr
XM_011515872.1:c.1552G>A (ELN) XP_011514174.1:p.Ala518Thr
XM_011515873.1:c.1549G>A (ELN) XP_011514175.1:p.Ala517Thr
XM_011515874.1:c.1540G>A (ELN) XP_011514176.1:p.Ala514Thr
XM_011515875.1:c.1525G>A (ELN) XP_011514177.1:p.Ala509Thr
XM_011515876.1:c.1606G>A (ELN) XP_011514178.1:p.Ala536Thr
XM_011515877.1:c.1495G>A (ELN) XP_011514179.1:p.Ala499Thr
XM_005250187.2:c.1555G>A (ELN) XP_005250244.1:p.Ala519Thr
XM_005250188.2:c.1549G>A (ELN) XP_005250245.1:p.Ala517Thr
XM_011515868.2:c.1606G>A (ELN) XP_011514170.1:p.Ala536Thr
XM_011515871.2:c.1564G>A (ELN) XP_011514173.1:p.Ala522Thr
XM_011515872.2:c.1552G>A (ELN) XP_011514174.1:p.Ala518Thr
XM_011515873.2:c.1549G>A (ELN) XP_011514175.1:p.Ala517Thr
XM_011515875.2:c.1525G>A (ELN) XP_011514177.1:p.Ala509Thr
XM_011515876.2:c.1606G>A (ELN) XP_011514178.1:p.Ala536Thr
XM_011515877.2:c.1495G>A (ELN) XP_011514179.1:p.Ala499Thr
XM_017011813.1:c.1519G>A (ELN) XP_016867302.1:p.Ala507Thr
XM_017011814.2:c.1507G>A (ELN) XP_016867303.1:p.Ala503Thr
XR_001745243.1:n.76-122C>T (ELN-AS1)
NM_000501.4:c.1591G>A (ELN) MANE Select NP_000492.2:p.Ala531Thr
NM_001081752.3:c.1504G>A (ELN) NP_001075221.1:p.Ala502Thr
NM_001081753.3:c.1549G>A (ELN) NP_001075222.1:p.Ala517Thr
NM_001081754.3:c.1606G>A (ELN) NP_001075223.1:p.Ala536Thr
NM_001081755.3:c.1534G>A (ELN) NP_001075224.1:p.Ala512Thr
NM_001278912.2:c.1591G>A (ELN) NP_001265841.1:p.Ala531Thr
NM_001278913.2:c.1348G>A (ELN) NP_001265842.1:p.Ala450Thr
NM_001278914.2:c.1519G>A (ELN) NP_001265843.1:p.Ala507Thr
NM_001278915.2:c.1609G>A (ELN) NP_001265844.1:p.Ala537Thr
NM_001278916.2:c.1477+107G>A (ELN) NP_001265845.1:n.1477+107G>A
NM_001278917.2:c.1561G>A (ELN) NP_001265846.1:p.Ala521Thr
NM_001278918.2:c.1324G>A (ELN) NP_001265847.1:p.Ala442Thr
NM_001278939.2:c.1678G>A (ELN) NP_001265868.1:p.Ala560Thr