Canonical Allele Identifier: CA1363079466

Gene: COL7A1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48570228A= , CM000665.2:g.48570228A=	GRCh38
NC_000003.11:g.48607661A= , CM000665.1:g.48607661A=	GRCh37
NC_000003.10:g.48582665A=	NCBI36
NG_007065.1:g.30025T= , LRG_286:g.30025T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000681320.1:c.7440+47T= MANE Select	ENSP00000506558.1:n.7440+47T=
ENST00000328333.12:c.7440+47T=	ENSP00000332371.8:n.7440+47T=
ENST00000422991.1:c.435+47T=	ENSP00000391608.1:n.435+47T=
ENST00000459756.5:n.214T=
ENST00000467985.1:n.237T=
ENST00000487017.5:n.4079+47T=
NM_000094.3:c.7440+47T= , LRG_286t1:c.7440+47T=	NP_000085.1:n.7440+47T=
XM_011533336.1:c.7467+47T=	XP_011531638.1:n.7467+47T=
XM_011533337.1:c.7440+47T=	XP_011531639.1:n.7440+47T=
XM_011533338.1:c.7408-50T=	XP_011531640.1:n.7408-50T=
XM_011533339.1:c.7467+47T=	XP_011531641.1:n.7467+47T=
XM_011533340.1:c.7432T=	XP_011531642.1:p.Cys2478=
XM_011533341.1:c.7406T=	XP_011531643.1:p.Leu2469=
XM_011533342.1:c.7382-50T=	XP_011531644.1:n.7382-50T=
XR_940369.1:n.7503+47T=
XR_940370.1:n.7503+47T=
XR_940371.1:n.7503+47T=
XR_940372.1:n.7477+47T=
XM_017005688.1:c.7381-50T=	XP_016861177.1:n.7381-50T=
XM_017005689.1:c.7440+47T=	XP_016861178.1:n.7440+47T=
XM_017005690.1:c.7405T=	XP_016861179.1:p.Cys2469=
XM_017005691.1:c.7379T=	XP_016861180.1:p.Leu2460=
XM_017005692.1:c.7355-50T=	XP_016861181.1:n.7355-50T=
XR_001740003.1:n.7476+47T=
XR_001740004.1:n.7476+47T=
XR_001740005.1:n.7476+47T=
XR_001740006.1:n.7450+47T=
NM_000094.4:c.7440+47T= MANE Select	NP_000085.1:n.7440+47T=