Canonical Allele Identifier: CA413847850

Gene: COL4A6

Linked Data

• MyVariant Identifiers: chrX:g.107400242C>A (hg19) ; chrX:g.108157012C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108157012C>A , CM000685.2:g.108157012C>A	GRCh38
NC_000023.10:g.107400242C>A , CM000685.1:g.107400242C>A	GRCh37
NC_000023.9:g.107286898C>A	NCBI36
NG_012059.2:g.287463G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000334504.12:c.5061G>T MANE Select	ENSP00000334733.7:p.Met1687Ile
ENST00000334504.11:c.5061G>T	ENSP00000334733.7:p.Met1687Ile
ENST00000372216.8:c.5064G>T	ENSP00000361290.4:p.Met1688Ile
ENST00000394872.6:c.5112G>T	ENSP00000378340.3:p.Met1704Ile
ENST00000538570.5:c.4890G>T	ENSP00000445236.1:p.Met1630Ile
ENST00000545689.2:c.5025G>T	ENSP00000443707.2:p.Met1675Ile
ENST00000621266.4:c.4989G>T	ENSP00000482970.1:p.Met1663Ile
NM_001287758.1:c.5112G>T	NP_001274687.1:p.Met1704Ile
NM_001287759.1:c.4989G>T	NP_001274688.1:p.Met1663Ile
NM_001287760.1:c.4890G>T	NP_001274689.1:p.Met1630Ile
NM_001847.3:c.5064G>T	NP_001838.2:p.Met1688Ile
NM_033641.3:c.5061G>T	NP_378667.1:p.Met1687Ile
XM_006724617.2:c.5115G>T	XP_006724680.1:p.Met1705Ile
XM_011530852.1:c.5043G>T	XP_011529154.1:p.Met1681Ile
XM_011530853.1:c.5031G>T	XP_011529155.1:p.Met1677Ile
XM_006724617.3:c.5115G>T	XP_006724680.1:p.Met1705Ile
XM_011530852.2:c.5043G>T	XP_011529154.1:p.Met1681Ile
XM_011530853.3:c.5031G>T	XP_011529155.1:p.Met1677Ile
NM_001847.4:c.5064G>T	NP_001838.2:p.Met1688Ile
NM_033641.4:c.5061G>T MANE Select	NP_378667.1:p.Met1687Ile
NM_001287758.2:c.5112G>T	NP_001274687.1:p.Met1704Ile
NM_001287759.2:c.4989G>T	NP_001274688.1:p.Met1663Ile
NM_001287760.2:c.4890G>T	NP_001274689.1:p.Met1630Ile