Canonical Allele Identifier: CA413848694
Gene: COL4A6 HGNC NCBI

Linked Data

dbSNP Id: rs761614268

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108157226G>A , CM000685.2:g.108157226G>A GRCh38
NC_000023.10:g.107400456G>A , CM000685.1:g.107400456G>A GRCh37
NC_000023.9:g.107287112G>A NCBI36
NG_012059.2:g.287249C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000334504.12:c.4847C>T MANE Select ENSP00000334733.7:p.Ser1616Phe
ENST00000334504.11:c.4847C>T ENSP00000334733.7:p.Ser1616Phe
ENST00000372216.8:c.4850C>T ENSP00000361290.4:p.Ser1617Phe
ENST00000394872.6:c.4898C>T ENSP00000378340.3:p.Ser1633Phe
ENST00000538570.5:c.4676C>T ENSP00000445236.1:p.Ser1559Phe
ENST00000545689.2:c.4811C>T ENSP00000443707.2:p.Ser1604Phe
ENST00000621266.4:c.4775C>T ENSP00000482970.1:p.Ser1592Phe
NM_001287758.1:c.4898C>T NP_001274687.1:p.Ser1633Phe
NM_001287759.1:c.4775C>T NP_001274688.1:p.Ser1592Phe
NM_001287760.1:c.4676C>T NP_001274689.1:p.Ser1559Phe
NM_001847.3:c.4850C>T NP_001838.2:p.Ser1617Phe
NM_033641.3:c.4847C>T NP_378667.1:p.Ser1616Phe
XM_006724617.2:c.4901C>T XP_006724680.1:p.Ser1634Phe
XM_011530852.1:c.4829C>T XP_011529154.1:p.Ser1610Phe
XM_011530853.1:c.4817C>T XP_011529155.1:p.Ser1606Phe
XM_006724617.3:c.4901C>T XP_006724680.1:p.Ser1634Phe
XM_011530852.2:c.4829C>T XP_011529154.1:p.Ser1610Phe
XM_011530853.3:c.4817C>T XP_011529155.1:p.Ser1606Phe
NM_001847.4:c.4850C>T NP_001838.2:p.Ser1617Phe
NM_033641.4:c.4847C>T MANE Select NP_378667.1:p.Ser1616Phe
NM_001287758.2:c.4898C>T NP_001274687.1:p.Ser1633Phe
NM_001287759.2:c.4775C>T NP_001274688.1:p.Ser1592Phe
NM_001287760.2:c.4676C>T NP_001274689.1:p.Ser1559Phe