Canonical Allele Identifier: CA907758652

Gene: COL7A1

Linked Data

• dbSNP Id: rs1377675777
• MyVariant Identifiers: chr3:g.48607501G>A (hg19) ; chr3:g.48570068G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48570068G>A , CM000665.2:g.48570068G>A	GRCh38
NC_000003.11:g.48607501G>A , CM000665.1:g.48607501G>A	GRCh37
NC_000003.10:g.48582505G>A	NCBI36
NG_007065.1:g.30185C>T , LRG_286:g.30185C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000681320.1:c.7485+66C>T MANE Select	ENSP00000506558.1:n.7485+66C>T
ENST00000328333.12:c.7485+66C>T	ENSP00000332371.8:n.7485+66C>T
ENST00000422991.1:c.480+66C>T	ENSP00000391608.1:n.480+66C>T
ENST00000459756.5:n.308+66C>T
ENST00000467985.1:n.331+66C>T
ENST00000487017.5:n.4124+66C>T
NM_000094.3:c.7485+66C>T , LRG_286t1:c.7485+66C>T	NP_000085.1:n.7485+66C>T
XM_011533336.1:c.7512+66C>T	XP_011531638.1:n.7512+66C>T
XM_011533337.1:c.7485+66C>T	XP_011531639.1:n.7485+66C>T
XM_011533338.1:c.7452+66C>T	XP_011531640.1:n.7452+66C>T
XM_011533339.1:c.7512+66C>T	XP_011531641.1:n.7512+66C>T
XM_011533342.1:c.*40+66C>T	XP_011531644.1:n.*40+66C>T
XR_940369.1:n.7548+66C>T
XR_940370.1:n.7548+66C>T
XR_940371.1:n.7548+66C>T
XR_940372.1:n.7522+66C>T
XM_017005688.1:c.7425+66C>T	XP_016861177.1:n.7425+66C>T
XM_017005689.1:c.7485+66C>T	XP_016861178.1:n.7485+66C>T
XM_017005692.1:c.*40+66C>T	XP_016861181.1:n.*40+66C>T
XR_001740003.1:n.7521+66C>T
XR_001740004.1:n.7521+66C>T
XR_001740005.1:n.7521+66C>T
XR_001740006.1:n.7495+66C>T
NM_000094.4:c.7485+66C>T MANE Select	NP_000085.1:n.7485+66C>T