Canonical Allele Identifier: CA2450541960

Gene: COL4A6

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108157132G= , CM000685.2:g.108157132G=	GRCh38
NC_000023.10:g.107400362G= , CM000685.1:g.107400362G=	GRCh37
NC_000023.9:g.107287018G=	NCBI36
NG_012059.2:g.287343C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334504.12:c.4941C= MANE Select	ENSP00000334733.7:p.Asn1647=
ENST00000334504.11:c.4941C=	ENSP00000334733.7:p.Asn1647=
ENST00000372216.8:c.4944C=	ENSP00000361290.4:p.Asn1648=
ENST00000394872.6:c.4992C=	ENSP00000378340.3:p.Asn1664=
ENST00000538570.5:c.4770C=	ENSP00000445236.1:p.Asn1590=
ENST00000545689.2:c.4905C=	ENSP00000443707.2:p.Asn1635=
ENST00000621266.4:c.4869C=	ENSP00000482970.1:p.Asn1623=
NM_001287758.1:c.4992C=	NP_001274687.1:p.Asn1664=
NM_001287759.1:c.4869C=	NP_001274688.1:p.Asn1623=
NM_001287760.1:c.4770C=	NP_001274689.1:p.Asn1590=
NM_001847.3:c.4944C=	NP_001838.2:p.Asn1648=
NM_033641.3:c.4941C=	NP_378667.1:p.Asn1647=
XM_006724617.2:c.4995C=	XP_006724680.1:p.Asn1665=
XM_011530852.1:c.4923C=	XP_011529154.1:p.Asn1641=
XM_011530853.1:c.4911C=	XP_011529155.1:p.Asn1637=
XM_006724617.3:c.4995C=	XP_006724680.1:p.Asn1665=
XM_011530852.2:c.4923C=	XP_011529154.1:p.Asn1641=
XM_011530853.3:c.4911C=	XP_011529155.1:p.Asn1637=
NM_001847.4:c.4944C=	NP_001838.2:p.Asn1648=
NM_033641.4:c.4941C= MANE Select	NP_378667.1:p.Asn1647=
NM_001287758.2:c.4992C=	NP_001274687.1:p.Asn1664=
NM_001287759.2:c.4869C=	NP_001274688.1:p.Asn1623=
NM_001287760.2:c.4770C=	NP_001274689.1:p.Asn1590=