Canonical Allele Identifier: CA2577587663

Gene: COL7A1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48568198C>A , CM000665.2:g.48568198C>A	GRCh38
NC_000003.11:g.48605631C>A , CM000665.1:g.48605631C>A	GRCh37
NC_000003.10:g.48580635C>A	NCBI36
NG_007065.1:g.32055G>T , LRG_286:g.32055G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681320.1:c.7795-28G>T MANE Select	ENSP00000506558.1:n.7795-28G>T
ENST00000328333.12:c.7795-28G>T	ENSP00000332371.8:n.7795-28G>T
ENST00000459756.5:n.618-28G>T
ENST00000467985.1:n.675G>T
ENST00000487017.5:n.4434-28G>T
NM_000094.3:c.7795-28G>T , LRG_286t1:c.7795-28G>T	NP_000085.1:n.7795-28G>T
XM_011533336.1:c.7822-28G>T	XP_011531638.1:n.7822-28G>T
XM_011533337.1:c.7795-28G>T	XP_011531639.1:n.7795-28G>T
XM_011533338.1:c.7762-28G>T	XP_011531640.1:n.7762-28G>T
XM_011533339.1:c.7856G>T	XP_011531641.1:p.Ter2619Leu
XR_940369.1:n.7858-28G>T
XR_940370.1:n.7858-28G>T
XR_940371.1:n.7858-28G>T
XR_940372.1:n.7832-28G>T
XM_017005688.1:c.7735-28G>T	XP_016861177.1:n.7735-28G>T
XM_017005689.1:c.7829G>T	XP_016861178.1:p.Ter2610Leu
XR_001740003.1:n.7831-28G>T
XR_001740004.1:n.7831-28G>T
XR_001740005.1:n.7831-28G>T
XR_001740006.1:n.7805-28G>T
NM_000094.4:c.7795-28G>T MANE Select	NP_000085.1:n.7795-28G>T