Canonical Allele Identifier: CA1363077198

Gene: COL7A1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48568510G= , CM000665.2:g.48568510G=	GRCh38
NC_000003.11:g.48605943G= , CM000665.1:g.48605943G=	GRCh37
NC_000003.10:g.48580947G=	NCBI36
NG_007065.1:g.31743C= , LRG_286:g.31743C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681320.1:c.7783C= MANE Select	ENSP00000506558.1:p.Pro2595=
ENST00000328333.12:c.7783C=	ENSP00000332371.8:p.Pro2595=
ENST00000459756.5:n.606C=
ENST00000467985.1:n.629C=
ENST00000487017.5:n.4422C=
NM_000094.3:c.7783C= , LRG_286t1:c.7783C=	NP_000085.1:p.Pro2595=
XM_011533336.1:c.7810C=	XP_011531638.1:p.Pro2604=
XM_011533337.1:c.7783C=	XP_011531639.1:p.Pro2595=
XM_011533338.1:c.7750C=	XP_011531640.1:p.Pro2584=
XM_011533339.1:c.7810C=	XP_011531641.1:p.Pro2604=
XR_940369.1:n.7846C=
XR_940370.1:n.7846C=
XR_940371.1:n.7846C=
XR_940372.1:n.7820C=
XM_017005688.1:c.7723C=	XP_016861177.1:p.Pro2575=
XM_017005689.1:c.7783C=	XP_016861178.1:p.Pro2595=
XR_001740003.1:n.7819C=
XR_001740004.1:n.7819C=
XR_001740005.1:n.7819C=
XR_001740006.1:n.7793C=
NM_000094.4:c.7783C= MANE Select	NP_000085.1:p.Pro2595=