Canonical Allele Identifier: CA518100711

Gene: COL4A6

Linked Data

• MyVariant Identifiers: chrX:g.107400305A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108157075A>T , CM000685.2:g.108157075A>T	GRCh38
NC_000023.10:g.107400305A>T , CM000685.1:g.107400305A>T	GRCh37
NC_000023.9:g.107286961A>T	NCBI36
NG_012059.2:g.287400T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334504.12:c.4998T>A MANE Select	ENSP00000334733.7:p.Pro1666=
ENST00000334504.11:c.4998T>A	ENSP00000334733.7:p.Pro1666=
ENST00000372216.8:c.5001T>A	ENSP00000361290.4:p.Pro1667=
ENST00000394872.6:c.5049T>A	ENSP00000378340.3:p.Pro1683=
ENST00000538570.5:c.4827T>A	ENSP00000445236.1:p.Pro1609=
ENST00000545689.2:c.4962T>A	ENSP00000443707.2:p.Pro1654=
ENST00000621266.4:c.4926T>A	ENSP00000482970.1:p.Pro1642=
NM_001287758.1:c.5049T>A	NP_001274687.1:p.Pro1683=
NM_001287759.1:c.4926T>A	NP_001274688.1:p.Pro1642=
NM_001287760.1:c.4827T>A	NP_001274689.1:p.Pro1609=
NM_001847.3:c.5001T>A	NP_001838.2:p.Pro1667=
NM_033641.3:c.4998T>A	NP_378667.1:p.Pro1666=
XM_006724617.2:c.5052T>A	XP_006724680.1:p.Pro1684=
XM_011530852.1:c.4980T>A	XP_011529154.1:p.Pro1660=
XM_011530853.1:c.4968T>A	XP_011529155.1:p.Pro1656=
XM_006724617.3:c.5052T>A	XP_006724680.1:p.Pro1684=
XM_011530852.2:c.4980T>A	XP_011529154.1:p.Pro1660=
XM_011530853.3:c.4968T>A	XP_011529155.1:p.Pro1656=
NM_001847.4:c.5001T>A	NP_001838.2:p.Pro1667=
NM_033641.4:c.4998T>A MANE Select	NP_378667.1:p.Pro1666=
NM_001287758.2:c.5049T>A	NP_001274687.1:p.Pro1683=
NM_001287759.2:c.4926T>A	NP_001274688.1:p.Pro1642=
NM_001287760.2:c.4827T>A	NP_001274689.1:p.Pro1609=