Canonical Allele Identifier: CA352636374

Gene: COL7A1

Linked Data

• MyVariant Identifiers: chr3:g.48603726A>G (hg19) ; chr3:g.48566293A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48566293A>G , CM000665.2:g.48566293A>G	GRCh38
NC_000003.11:g.48603726A>G , CM000665.1:g.48603726A>G	GRCh37
NC_000003.10:g.48578730A>G	NCBI36
NG_007065.1:g.33960T>C , LRG_286:g.33960T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000681320.1:c.8381T>C MANE Select	ENSP00000506558.1:p.Val2794Ala
ENST00000328333.12:c.8381T>C	ENSP00000332371.8:p.Val2794Ala
ENST00000487017.5:n.5020T>C
NM_000094.3:c.8381T>C , LRG_286t1:c.8381T>C	NP_000085.1:p.Val2794Ala
XM_011533336.1:c.8408T>C	XP_011531638.1:p.Val2803Ala
XM_011533337.1:c.8381T>C	XP_011531639.1:p.Val2794Ala
XM_011533338.1:c.8348T>C	XP_011531640.1:p.Val2783Ala
XR_940369.1:n.8444T>C
XR_940370.1:n.8444T>C
XR_940371.1:n.8444T>C
XM_017005688.1:c.8321T>C	XP_016861177.1:p.Val2774Ala
XR_001740003.1:n.8417T>C
XR_001740004.1:n.8417T>C
XR_001740005.1:n.8417T>C
NM_000094.4:c.8381T>C MANE Select	NP_000085.1:p.Val2794Ala