Canonical Allele Identifier: CA352643044

Gene: COL7A1

Linked Data

• MyVariant Identifiers: chr3:g.48606249A>C (hg19) ; chr3:g.48568816A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48568816A>C , CM000665.2:g.48568816A>C	GRCh38
NC_000003.11:g.48606249A>C , CM000665.1:g.48606249A>C	GRCh37
NC_000003.10:g.48581253A>C	NCBI36
NG_007065.1:g.31437T>G , LRG_286:g.31437T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681320.1:c.7726T>G MANE Select	ENSP00000506558.1:p.Leu2576Val
ENST00000328333.12:c.7726T>G	ENSP00000332371.8:p.Leu2576Val
ENST00000459756.5:n.549T>G
ENST00000467985.1:n.572T>G
ENST00000487017.5:n.4365T>G
NM_000094.3:c.7726T>G , LRG_286t1:c.7726T>G	NP_000085.1:p.Leu2576Val
XM_011533336.1:c.7753T>G	XP_011531638.1:p.Leu2585Val
XM_011533337.1:c.7726T>G	XP_011531639.1:p.Leu2576Val
XM_011533338.1:c.7693T>G	XP_011531640.1:p.Leu2565Val
XM_011533339.1:c.7753T>G	XP_011531641.1:p.Leu2585Val
XR_940369.1:n.7789T>G
XR_940370.1:n.7789T>G
XR_940371.1:n.7789T>G
XR_940372.1:n.7763T>G
XM_017005688.1:c.7666T>G	XP_016861177.1:p.Leu2556Val
XM_017005689.1:c.7726T>G	XP_016861178.1:p.Leu2576Val
XR_001740003.1:n.7762T>G
XR_001740004.1:n.7762T>G
XR_001740005.1:n.7762T>G
XR_001740006.1:n.7736T>G
NM_000094.4:c.7726T>G MANE Select	NP_000085.1:p.Leu2576Val