Canonical Allele Identifier: CA413848179

Gene: COL4A6

Linked Data

• gnomAD v4: X-108157101-C-A
• MyVariant Identifiers: chrX:g.107400331C>A (hg19) ; chrX:g.108157101C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108157101C>A , CM000685.2:g.108157101C>A	GRCh38
NC_000023.10:g.107400331C>A , CM000685.1:g.107400331C>A	GRCh37
NC_000023.9:g.107286987C>A	NCBI36
NG_012059.2:g.287374G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334504.12:c.4972G>T MANE Select	ENSP00000334733.7:p.Glu1658Ter
ENST00000334504.11:c.4972G>T	ENSP00000334733.7:p.Glu1658Ter
ENST00000372216.8:c.4975G>T	ENSP00000361290.4:p.Glu1659Ter
ENST00000394872.6:c.5023G>T	ENSP00000378340.3:p.Glu1675Ter
ENST00000538570.5:c.4801G>T	ENSP00000445236.1:p.Glu1601Ter
ENST00000545689.2:c.4936G>T	ENSP00000443707.2:p.Glu1646Ter
ENST00000621266.4:c.4900G>T	ENSP00000482970.1:p.Glu1634Ter
NM_001287758.1:c.5023G>T	NP_001274687.1:p.Glu1675Ter
NM_001287759.1:c.4900G>T	NP_001274688.1:p.Glu1634Ter
NM_001287760.1:c.4801G>T	NP_001274689.1:p.Glu1601Ter
NM_001847.3:c.4975G>T	NP_001838.2:p.Glu1659Ter
NM_033641.3:c.4972G>T	NP_378667.1:p.Glu1658Ter
XM_006724617.2:c.5026G>T	XP_006724680.1:p.Glu1676Ter
XM_011530852.1:c.4954G>T	XP_011529154.1:p.Glu1652Ter
XM_011530853.1:c.4942G>T	XP_011529155.1:p.Glu1648Ter
XM_006724617.3:c.5026G>T	XP_006724680.1:p.Glu1676Ter
XM_011530852.2:c.4954G>T	XP_011529154.1:p.Glu1652Ter
XM_011530853.3:c.4942G>T	XP_011529155.1:p.Glu1648Ter
NM_001847.4:c.4975G>T	NP_001838.2:p.Glu1659Ter
NM_033641.4:c.4972G>T MANE Select	NP_378667.1:p.Glu1658Ter
NM_001287758.2:c.5023G>T	NP_001274687.1:p.Glu1675Ter
NM_001287759.2:c.4900G>T	NP_001274688.1:p.Glu1634Ter
NM_001287760.2:c.4801G>T	NP_001274689.1:p.Glu1601Ter