Canonical Allele Identifier: CA1363076188

Gene: COL7A1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48567819G= , CM000665.2:g.48567819G=	GRCh38
NC_000003.11:g.48605252G= , CM000665.1:g.48605252G=	GRCh37
NC_000003.10:g.48580256G=	NCBI36
NG_007065.1:g.32434C= , LRG_286:g.32434C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681320.1:c.7929+19C= MANE Select	ENSP00000506558.1:n.7929+19C=
ENST00000328333.12:c.7929+19C=	ENSP00000332371.8:n.7929+19C=
ENST00000459756.5:n.752+19C=
ENST00000487017.5:n.4568+19C=
NM_000094.3:c.7929+19C= , LRG_286t1:c.7929+19C=	NP_000085.1:n.7929+19C=
XM_011533336.1:c.7956+19C=	XP_011531638.1:n.7956+19C=
XM_011533337.1:c.7929+19C=	XP_011531639.1:n.7929+19C=
XM_011533338.1:c.7896+19C=	XP_011531640.1:n.7896+19C=
XR_940369.1:n.7992+19C=
XR_940370.1:n.7992+19C=
XR_940371.1:n.7992+19C=
XM_017005688.1:c.7869+19C=	XP_016861177.1:n.7869+19C=
XR_001740003.1:n.7965+19C=
XR_001740004.1:n.7965+19C=
XR_001740005.1:n.7965+19C=
NM_000094.4:c.7929+19C= MANE Select	NP_000085.1:n.7929+19C=