Canonical Allele Identifier: CA518100932

Gene: COL4A6

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108159513C>T , CM000685.2:g.108159513C>T	GRCh38
NC_000023.10:g.107402743C>T , CM000685.1:g.107402743C>T	GRCh37
NC_000023.9:g.107289399C>T	NCBI36
NG_012059.2:g.284962G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334504.12:c.4761G>A MANE Select	ENSP00000334733.7:p.Pro1587=
ENST00000334504.11:c.4761G>A	ENSP00000334733.7:p.Pro1587=
ENST00000372216.8:c.4764G>A	ENSP00000361290.4:p.Pro1588=
ENST00000394872.6:c.4812G>A	ENSP00000378340.3:p.Pro1604=
ENST00000538570.5:c.4590G>A	ENSP00000445236.1:p.Pro1530=
ENST00000545689.2:c.4725G>A	ENSP00000443707.2:p.Pro1575=
ENST00000621266.4:c.4689G>A	ENSP00000482970.1:p.Pro1563=
NM_001287758.1:c.4812G>A	NP_001274687.1:p.Pro1604=
NM_001287759.1:c.4689G>A	NP_001274688.1:p.Pro1563=
NM_001287760.1:c.4590G>A	NP_001274689.1:p.Pro1530=
NM_001847.3:c.4764G>A	NP_001838.2:p.Pro1588=
NM_033641.3:c.4761G>A	NP_378667.1:p.Pro1587=
XM_006724617.2:c.4815G>A	XP_006724680.1:p.Pro1605=
XM_011530852.1:c.4743G>A	XP_011529154.1:p.Pro1581=
XM_011530853.1:c.4731G>A	XP_011529155.1:p.Pro1577=
XM_006724617.3:c.4815G>A	XP_006724680.1:p.Pro1605=
XM_011530852.2:c.4743G>A	XP_011529154.1:p.Pro1581=
XM_011530853.3:c.4731G>A	XP_011529155.1:p.Pro1577=
NM_001847.4:c.4764G>A	NP_001838.2:p.Pro1588=
NM_033641.4:c.4761G>A MANE Select	NP_378667.1:p.Pro1587=
NM_001287758.2:c.4812G>A	NP_001274687.1:p.Pro1604=
NM_001287759.2:c.4689G>A	NP_001274688.1:p.Pro1563=
NM_001287760.2:c.4590G>A	NP_001274689.1:p.Pro1530=