Canonical Allele Identifier: CA352643053

Gene: COL7A1

Linked Data

• gnomAD v4: 3-48568818-C-G
• MyVariant Identifiers: chr3:g.48606251C>G (hg19) ; chr3:g.48568818C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48568818C>G , CM000665.2:g.48568818C>G	GRCh38
NC_000003.11:g.48606251C>G , CM000665.1:g.48606251C>G	GRCh37
NC_000003.10:g.48581255C>G	NCBI36
NG_007065.1:g.31435G>C , LRG_286:g.31435G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681320.1:c.7724G>C MANE Select	ENSP00000506558.1:p.Gly2575Ala
ENST00000328333.12:c.7724G>C	ENSP00000332371.8:p.Gly2575Ala
ENST00000459756.5:n.547G>C
ENST00000467985.1:n.570G>C
ENST00000487017.5:n.4363G>C
NM_000094.3:c.7724G>C , LRG_286t1:c.7724G>C	NP_000085.1:p.Gly2575Ala
XM_011533336.1:c.7751G>C	XP_011531638.1:p.Gly2584Ala
XM_011533337.1:c.7724G>C	XP_011531639.1:p.Gly2575Ala
XM_011533338.1:c.7691G>C	XP_011531640.1:p.Gly2564Ala
XM_011533339.1:c.7751G>C	XP_011531641.1:p.Gly2584Ala
XR_940369.1:n.7787G>C
XR_940370.1:n.7787G>C
XR_940371.1:n.7787G>C
XR_940372.1:n.7761G>C
XM_017005688.1:c.7664G>C	XP_016861177.1:p.Gly2555Ala
XM_017005689.1:c.7724G>C	XP_016861178.1:p.Gly2575Ala
XR_001740003.1:n.7760G>C
XR_001740004.1:n.7760G>C
XR_001740005.1:n.7760G>C
XR_001740006.1:n.7734G>C
NM_000094.4:c.7724G>C MANE Select	NP_000085.1:p.Gly2575Ala