Canonical Allele Identifier: CA2502150925
Gene: COL7A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48566602C>A , CM000665.2:g.48566602C>A GRCh38
NC_000003.11:g.48604035C>A , CM000665.1:g.48604035C>A GRCh37
NC_000003.10:g.48579039C>A NCBI36
NG_007065.1:g.33651G>T , LRG_286:g.33651G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000681320.1:c.8305-39G>T MANE Select ENSP00000506558.1:n.8305-39G>T
ENST00000328333.12:c.8305-39G>T ENSP00000332371.8:n.8305-39G>T
ENST00000474432.1:n.705-39G>T
ENST00000487017.5:n.4944-39G>T
NM_000094.3:c.8305-39G>T , LRG_286t1:c.8305-39G>T NP_000085.1:n.8305-39G>T
XM_011533336.1:c.8332-39G>T XP_011531638.1:n.8332-39G>T
XM_011533337.1:c.8305-39G>T XP_011531639.1:n.8305-39G>T
XM_011533338.1:c.8272-39G>T XP_011531640.1:n.8272-39G>T
XR_940369.1:n.8368-39G>T
XR_940370.1:n.8368-39G>T
XR_940371.1:n.8368-39G>T
XM_017005688.1:c.8245-39G>T XP_016861177.1:n.8245-39G>T
XR_001740003.1:n.8341-39G>T
XR_001740004.1:n.8341-39G>T
XR_001740005.1:n.8341-39G>T
NM_000094.4:c.8305-39G>T MANE Select NP_000085.1:n.8305-39G>T