Canonical Allele Identifier: CA352641321

Gene: COL7A1

Linked Data

• MyVariant Identifiers: chr3:g.48605174C>A (hg19) ; chr3:g.48567741C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48567741C>A , CM000665.2:g.48567741C>A	GRCh38
NC_000003.11:g.48605174C>A , CM000665.1:g.48605174C>A	GRCh37
NC_000003.10:g.48580178C>A	NCBI36
NG_007065.1:g.32512G>T , LRG_286:g.32512G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681320.1:c.7952G>T MANE Select	ENSP00000506558.1:p.Arg2651Leu
ENST00000328333.12:c.7952G>T	ENSP00000332371.8:p.Arg2651Leu
ENST00000459756.5:n.775G>T
ENST00000487017.5:n.4591G>T
NM_000094.3:c.7952G>T , LRG_286t1:c.7952G>T	NP_000085.1:p.Arg2651Leu
XM_011533336.1:c.7979G>T	XP_011531638.1:p.Arg2660Leu
XM_011533337.1:c.7952G>T	XP_011531639.1:p.Arg2651Leu
XM_011533338.1:c.7919G>T	XP_011531640.1:p.Arg2640Leu
XR_940369.1:n.8015G>T
XR_940370.1:n.8015G>T
XR_940371.1:n.8015G>T
XM_017005688.1:c.7892G>T	XP_016861177.1:p.Arg2631Leu
XR_001740003.1:n.7988G>T
XR_001740004.1:n.7988G>T
XR_001740005.1:n.7988G>T
NM_000094.4:c.7952G>T MANE Select	NP_000085.1:p.Arg2651Leu