Canonical Allele Identifier: CA1332795980

Gene: COL4A3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.227164688G= , CM000664.2:g.227164688G=	GRCh38
NC_000002.11:g.228029404G= , CM000664.1:g.228029404G=	GRCh37
NC_000002.10:g.227737648G=	NCBI36
NG_011591.1:g.5124G= , LRG_230:g.5124G=
NG_011592.1:g.4872C= , LRG_231:g.4872C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396578.8:c.-39G= MANE Select	ENSP00000379823.3:n.-39G=
ENST00000396578.7:c.-39G=	ENSP00000379823.3:n.-39G=
NM_000091.4:c.-39G= , LRG_230t1:c.-39G=	NP_000082.2:n.-39G=
XM_005246276.2:c.-39G=	XP_005246333.1:n.-39G=
XM_005246277.2:c.-39G=	XP_005246334.1:n.-39G=
XM_005246280.2:c.-39G=	XP_005246337.1:n.-39G=
XM_006712245.2:c.-39G=	XP_006712308.1:n.-39G=
XM_011510555.1:c.-39G=	XP_011508857.1:n.-39G=
XR_241280.2:n.100G=
XM_005246277.3:c.-39G=	XP_005246334.1:n.-39G=
XM_005246280.3:c.-39G=	XP_005246337.1:n.-39G=
XM_006712245.3:c.-39G=	XP_006712308.1:n.-39G=
XM_017003295.1:c.-39G=	XP_016858784.1:n.-39G=
XR_001738601.1:n.100G=
XR_241280.3:n.100G=
NM_000091.5:c.-39G= MANE Select	NP_000082.2:n.-39G=