Canonical Allele Identifier: CA2577587633

Gene: COL7A1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48567678G>A , CM000665.2:g.48567678G>A	GRCh38
NC_000003.11:g.48605111G>A , CM000665.1:g.48605111G>A	GRCh37
NC_000003.10:g.48580115G>A	NCBI36
NG_007065.1:g.32575C>T , LRG_286:g.32575C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681320.1:c.7983+32C>T MANE Select	ENSP00000506558.1:n.7983+32C>T
ENST00000328333.12:c.7983+32C>T	ENSP00000332371.8:n.7983+32C>T
ENST00000487017.5:n.4622+32C>T
NM_000094.3:c.7983+32C>T , LRG_286t1:c.7983+32C>T	NP_000085.1:n.7983+32C>T
XM_011533336.1:c.8010+32C>T	XP_011531638.1:n.8010+32C>T
XM_011533337.1:c.7983+32C>T	XP_011531639.1:n.7983+32C>T
XM_011533338.1:c.7950+32C>T	XP_011531640.1:n.7950+32C>T
XR_940369.1:n.8046+32C>T
XR_940370.1:n.8046+32C>T
XR_940371.1:n.8046+32C>T
XM_017005688.1:c.7923+32C>T	XP_016861177.1:n.7923+32C>T
XR_001740003.1:n.8019+32C>T
XR_001740004.1:n.8019+32C>T
XR_001740005.1:n.8019+32C>T
NM_000094.4:c.7983+32C>T MANE Select	NP_000085.1:n.7983+32C>T