Canonical Allele Identifier: CA10487099
Gene: COL4A6 HGNC NCBI

Linked Data

dbSNP Id: rs761614268

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000334504.12:c.4847C>A MANE Select ENSP00000334733.7:p.Ser1616Tyr
ENST00000334504.11:c.4847C>A ENSP00000334733.7:p.Ser1616Tyr
ENST00000372216.8:c.4850C>A ENSP00000361290.4:p.Ser1617Tyr
ENST00000394872.6:c.4898C>A ENSP00000378340.3:p.Ser1633Tyr
ENST00000538570.5:c.4676C>A ENSP00000445236.1:p.Ser1559Tyr
ENST00000545689.2:c.4811C>A ENSP00000443707.2:p.Ser1604Tyr
ENST00000621266.4:c.4775C>A ENSP00000482970.1:p.Ser1592Tyr
NM_001287758.1:c.4898C>A NP_001274687.1:p.Ser1633Tyr
NM_001287759.1:c.4775C>A NP_001274688.1:p.Ser1592Tyr
NM_001287760.1:c.4676C>A NP_001274689.1:p.Ser1559Tyr
NM_001847.3:c.4850C>A NP_001838.2:p.Ser1617Tyr
NM_033641.3:c.4847C>A NP_378667.1:p.Ser1616Tyr
XM_006724617.2:c.4901C>A XP_006724680.1:p.Ser1634Tyr
XM_011530852.1:c.4829C>A XP_011529154.1:p.Ser1610Tyr
XM_011530853.1:c.4817C>A XP_011529155.1:p.Ser1606Tyr
XM_006724617.3:c.4901C>A XP_006724680.1:p.Ser1634Tyr
XM_011530852.2:c.4829C>A XP_011529154.1:p.Ser1610Tyr
XM_011530853.3:c.4817C>A XP_011529155.1:p.Ser1606Tyr
NM_001847.4:c.4850C>A NP_001838.2:p.Ser1617Tyr
NM_033641.4:c.4847C>A MANE Select NP_378667.1:p.Ser1616Tyr
NM_001287758.2:c.4898C>A NP_001274687.1:p.Ser1633Tyr
NM_001287759.2:c.4775C>A NP_001274688.1:p.Ser1592Tyr
NM_001287760.2:c.4676C>A NP_001274689.1:p.Ser1559Tyr