Canonical Allele Identifier: CA433533341
Gene: COL7A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.48606249A>G (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000681320.1:c.7726T>C MANE Select ENSP00000506558.1:p.Leu2576=
ENST00000328333.12:c.7726T>C ENSP00000332371.8:p.Leu2576=
ENST00000459756.5:n.549T>C
ENST00000467985.1:n.572T>C
ENST00000487017.5:n.4365T>C
NM_000094.3:c.7726T>C , LRG_286t1:c.7726T>C NP_000085.1:p.Leu2576=
XM_011533336.1:c.7753T>C XP_011531638.1:p.Leu2585=
XM_011533337.1:c.7726T>C XP_011531639.1:p.Leu2576=
XM_011533338.1:c.7693T>C XP_011531640.1:p.Leu2565=
XM_011533339.1:c.7753T>C XP_011531641.1:p.Leu2585=
XR_940369.1:n.7789T>C
XR_940370.1:n.7789T>C
XR_940371.1:n.7789T>C
XR_940372.1:n.7763T>C
XM_017005688.1:c.7666T>C XP_016861177.1:p.Leu2556=
XM_017005689.1:c.7726T>C XP_016861178.1:p.Leu2576=
XR_001740003.1:n.7762T>C
XR_001740004.1:n.7762T>C
XR_001740005.1:n.7762T>C
XR_001740006.1:n.7736T>C
NM_000094.4:c.7726T>C MANE Select NP_000085.1:p.Leu2576=