Canonical Allele Identifier: CA2378498

Gene: COL7A1

Linked Data

• dbSNP Id: rs777607211
• ExAC: 3:48607645 G / T
• gnomAD v2: 3-48607645-G-T
• MyVariant Identifiers: chr3:g.48607645G>T (hg19) ; chr3:g.48570212G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48570212G>T , CM000665.2:g.48570212G>T	GRCh38
NC_000003.11:g.48607645G>T , CM000665.1:g.48607645G>T	GRCh37
NC_000003.10:g.48582649G>T	NCBI36
NG_007065.1:g.30041C>A , LRG_286:g.30041C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000681320.1:c.7441-34C>A MANE Select	ENSP00000506558.1:n.7441-34C>A
ENST00000328333.12:c.7441-34C>A	ENSP00000332371.8:n.7441-34C>A
ENST00000422991.1:c.436-34C>A	ENSP00000391608.1:n.436-34C>A
ENST00000459756.5:n.230C>A
ENST00000467985.1:n.253C>A
ENST00000487017.5:n.4080-34C>A
NM_000094.3:c.7441-34C>A , LRG_286t1:c.7441-34C>A	NP_000085.1:n.7441-34C>A
XM_011533336.1:c.7468-34C>A	XP_011531638.1:n.7468-34C>A
XM_011533337.1:c.7441-34C>A	XP_011531639.1:n.7441-34C>A
XM_011533338.1:c.7408-34C>A	XP_011531640.1:n.7408-34C>A
XM_011533339.1:c.7468-34C>A	XP_011531641.1:n.7468-34C>A
XM_011533340.1:c.*8C>A	XP_011531642.1:n.*8C>A
XM_011533341.1:c.7422C>A	XP_011531643.1:p.Asn2474Lys
XM_011533342.1:c.7382-34C>A	XP_011531644.1:n.7382-34C>A
XR_940369.1:n.7504-34C>A
XR_940370.1:n.7504-34C>A
XR_940371.1:n.7504-34C>A
XR_940372.1:n.7478-34C>A
XM_017005688.1:c.7381-34C>A	XP_016861177.1:n.7381-34C>A
XM_017005689.1:c.7441-34C>A	XP_016861178.1:n.7441-34C>A
XM_017005690.1:c.*8C>A	XP_016861179.1:n.*8C>A
XM_017005691.1:c.7395C>A	XP_016861180.1:p.Asn2465Lys
XM_017005692.1:c.7355-34C>A	XP_016861181.1:n.7355-34C>A
XR_001740003.1:n.7477-34C>A
XR_001740004.1:n.7477-34C>A
XR_001740005.1:n.7477-34C>A
XR_001740006.1:n.7451-34C>A
NM_000094.4:c.7441-34C>A MANE Select	NP_000085.1:n.7441-34C>A