Canonical Allele Identifier: CA433532815

Gene: COL7A1

Linked Data

• MyVariant Identifiers: chr3:g.48605158T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48567725T>G , CM000665.2:g.48567725T>G	GRCh38
NC_000003.11:g.48605158T>G , CM000665.1:g.48605158T>G	GRCh37
NC_000003.10:g.48580162T>G	NCBI36
NG_007065.1:g.32528A>C , LRG_286:g.32528A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681320.1:c.7968A>C MANE Select	ENSP00000506558.1:p.Gly2656=
ENST00000328333.12:c.7968A>C	ENSP00000332371.8:p.Gly2656=
ENST00000459756.5:n.791A>C
ENST00000487017.5:n.4607A>C
NM_000094.3:c.7968A>C , LRG_286t1:c.7968A>C	NP_000085.1:p.Gly2656=
XM_011533336.1:c.7995A>C	XP_011531638.1:p.Gly2665=
XM_011533337.1:c.7968A>C	XP_011531639.1:p.Gly2656=
XM_011533338.1:c.7935A>C	XP_011531640.1:p.Gly2645=
XR_940369.1:n.8031A>C
XR_940370.1:n.8031A>C
XR_940371.1:n.8031A>C
XM_017005688.1:c.7908A>C	XP_016861177.1:p.Gly2636=
XR_001740003.1:n.8004A>C
XR_001740004.1:n.8004A>C
XR_001740005.1:n.8004A>C
NM_000094.4:c.7968A>C MANE Select	NP_000085.1:p.Gly2656=