Canonical Allele Identifier: CA1363079619

Gene: COL7A1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48570318C= , CM000665.2:g.48570318C=	GRCh38
NC_000003.11:g.48607751C= , CM000665.1:g.48607751C=	GRCh37
NC_000003.10:g.48582755C=	NCBI36
NG_007065.1:g.29935G= , LRG_286:g.29935G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000681320.1:c.7397G= MANE Select	ENSP00000506558.1:p.Gly2466=
ENST00000328333.12:c.7397G=	ENSP00000332371.8:p.Gly2466=
ENST00000422991.1:c.392G=	ENSP00000391608.1:p.Gly131=
ENST00000459756.5:n.124G=
ENST00000467985.1:n.147G=
ENST00000487017.5:n.4036G=
NM_000094.3:c.7397G= , LRG_286t1:c.7397G=	NP_000085.1:p.Gly2466=
XM_011533336.1:c.7424G=	XP_011531638.1:p.Gly2475=
XM_011533337.1:c.7397G=	XP_011531639.1:p.Gly2466=
XM_011533338.1:c.7408-140G=	XP_011531640.1:n.7408-140G=
XM_011533339.1:c.7424G=	XP_011531641.1:p.Gly2475=
XM_011533340.1:c.7408-66G=	XP_011531642.1:n.7408-66G=
XM_011533341.1:c.7382-66G=	XP_011531643.1:n.7382-66G=
XM_011533342.1:c.7382-140G=	XP_011531644.1:n.7382-140G=
XR_940369.1:n.7460G=
XR_940370.1:n.7460G=
XR_940371.1:n.7460G=
XR_940372.1:n.7434G=
XM_017005688.1:c.7381-140G=	XP_016861177.1:n.7381-140G=
XM_017005689.1:c.7397G=	XP_016861178.1:p.Gly2466=
XM_017005690.1:c.7381-66G=	XP_016861179.1:n.7381-66G=
XM_017005691.1:c.7355-66G=	XP_016861180.1:n.7355-66G=
XM_017005692.1:c.7355-140G=	XP_016861181.1:n.7355-140G=
XR_001740003.1:n.7433G=
XR_001740004.1:n.7433G=
XR_001740005.1:n.7433G=
XR_001740006.1:n.7407G=
NM_000094.4:c.7397G= MANE Select	NP_000085.1:p.Gly2466=