Canonical Allele Identifier: CA2830665830

Gene: COL7A1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48568349A>G , CM000665.2:g.48568349A>G	GRCh38
NC_000003.11:g.48605782A>G , CM000665.1:g.48605782A>G	GRCh37
NC_000003.10:g.48580786A>G	NCBI36
NG_007065.1:g.31904T>C , LRG_286:g.31904T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681320.1:c.7794+150T>C MANE Select	ENSP00000506558.1:n.7794+150T>C
ENST00000328333.12:c.7794+150T>C	ENSP00000332371.8:n.7794+150T>C
ENST00000459756.5:n.617+150T>C
ENST00000467985.1:n.641-117T>C
ENST00000487017.5:n.4433+150T>C
NM_000094.3:c.7794+150T>C , LRG_286t1:c.7794+150T>C	NP_000085.1:n.7794+150T>C
XM_011533336.1:c.7821+150T>C	XP_011531638.1:n.7821+150T>C
XM_011533337.1:c.7794+150T>C	XP_011531639.1:n.7794+150T>C
XM_011533338.1:c.7761+150T>C	XP_011531640.1:n.7761+150T>C
XM_011533339.1:c.7822-117T>C	XP_011531641.1:n.7822-117T>C
XR_940369.1:n.7857+150T>C
XR_940370.1:n.7857+150T>C
XR_940371.1:n.7857+150T>C
XR_940372.1:n.7831+150T>C
XM_017005688.1:c.7734+150T>C	XP_016861177.1:n.7734+150T>C
XM_017005689.1:c.7795-117T>C	XP_016861178.1:n.7795-117T>C
XR_001740003.1:n.7830+150T>C
XR_001740004.1:n.7830+150T>C
XR_001740005.1:n.7830+150T>C
XR_001740006.1:n.7804+150T>C
NM_000094.4:c.7794+150T>C MANE Select	NP_000085.1:n.7794+150T>C