Canonical Allele Identifier: CA1363080635

Gene: COL7A1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48566621A= , CM000665.2:g.48566621A=	GRCh38
NC_000003.11:g.48604054A= , CM000665.1:g.48604054A=	GRCh37
NC_000003.10:g.48579058A=	NCBI36
NG_007065.1:g.33632T= , LRG_286:g.33632T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000681320.1:c.8304+39T= MANE Select	ENSP00000506558.1:n.8304+39T=
ENST00000328333.12:c.8304+39T=	ENSP00000332371.8:n.8304+39T=
ENST00000474432.1:n.704+39T=
ENST00000487017.5:n.4943+39T=
NM_000094.3:c.8304+39T= , LRG_286t1:c.8304+39T=	NP_000085.1:n.8304+39T=
XM_011533336.1:c.8331+39T=	XP_011531638.1:n.8331+39T=
XM_011533337.1:c.8304+39T=	XP_011531639.1:n.8304+39T=
XM_011533338.1:c.8271+39T=	XP_011531640.1:n.8271+39T=
XR_940369.1:n.8367+39T=
XR_940370.1:n.8367+39T=
XR_940371.1:n.8367+39T=
XM_017005688.1:c.8244+39T=	XP_016861177.1:n.8244+39T=
XR_001740003.1:n.8340+39T=
XR_001740004.1:n.8340+39T=
XR_001740005.1:n.8340+39T=
NM_000094.4:c.8304+39T= MANE Select	NP_000085.1:n.8304+39T=