Canonical Allele Identifier: CA413848306
Gene: COL4A6 HGNC NCBI

Linked Data

dbSNP Id: rs1296923704

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108157141G>T , CM000685.2:g.108157141G>T GRCh38
NC_000023.10:g.107400371G>T , CM000685.1:g.107400371G>T GRCh37
NC_000023.9:g.107287027G>T NCBI36
NG_012059.2:g.287334C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000334504.12:c.4932C>A MANE Select ENSP00000334733.7:p.Tyr1644Ter
ENST00000334504.11:c.4932C>A ENSP00000334733.7:p.Tyr1644Ter
ENST00000372216.8:c.4935C>A ENSP00000361290.4:p.Tyr1645Ter
ENST00000394872.6:c.4983C>A ENSP00000378340.3:p.Tyr1661Ter
ENST00000538570.5:c.4761C>A ENSP00000445236.1:p.Tyr1587Ter
ENST00000545689.2:c.4896C>A ENSP00000443707.2:p.Tyr1632Ter
ENST00000621266.4:c.4860C>A ENSP00000482970.1:p.Tyr1620Ter
NM_001287758.1:c.4983C>A NP_001274687.1:p.Tyr1661Ter
NM_001287759.1:c.4860C>A NP_001274688.1:p.Tyr1620Ter
NM_001287760.1:c.4761C>A NP_001274689.1:p.Tyr1587Ter
NM_001847.3:c.4935C>A NP_001838.2:p.Tyr1645Ter
NM_033641.3:c.4932C>A NP_378667.1:p.Tyr1644Ter
XM_006724617.2:c.4986C>A XP_006724680.1:p.Tyr1662Ter
XM_011530852.1:c.4914C>A XP_011529154.1:p.Tyr1638Ter
XM_011530853.1:c.4902C>A XP_011529155.1:p.Tyr1634Ter
XM_006724617.3:c.4986C>A XP_006724680.1:p.Tyr1662Ter
XM_011530852.2:c.4914C>A XP_011529154.1:p.Tyr1638Ter
XM_011530853.3:c.4902C>A XP_011529155.1:p.Tyr1634Ter
NM_001847.4:c.4935C>A NP_001838.2:p.Tyr1645Ter
NM_033641.4:c.4932C>A MANE Select NP_378667.1:p.Tyr1644Ter
NM_001287758.2:c.4983C>A NP_001274687.1:p.Tyr1661Ter
NM_001287759.2:c.4860C>A NP_001274688.1:p.Tyr1620Ter
NM_001287760.2:c.4761C>A NP_001274689.1:p.Tyr1587Ter