Canonical Allele Identifier: CA257965
Community Standard Title: NM_000094.4(COL7A1):c.8245G>A (p.Gly2749Arg)
Gene: COL7A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48566719C>T , CM000665.2:g.48566719C>T GRCh38
NC_000003.11:g.48604152C>T , CM000665.1:g.48604152C>T GRCh37
NC_000003.10:g.48579156C>T NCBI36
NG_007065.1:g.33534G>A , LRG_286:g.33534G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000094.4:c.8245G>A MANE Select NP_000085.1:p.Gly2749Arg
ENST00000681320.1:c.8245G>A MANE Select ENSP00000506558.1:p.Gly2749Arg
NM_000094.3:c.8245G>A , LRG_286t1:c.8245G>A NP_000085.1:p.Gly2749Arg
ENST00000328333.12:c.8245G>A ENSP00000332371.8:p.Gly2749Arg
ENST00000474432.1:n.645G>A
ENST00000487017.5:n.4884G>A
XM_011533336.1:c.8272G>A XP_011531638.1:p.Gly2758Arg
XM_011533337.1:c.8245G>A XP_011531639.1:p.Gly2749Arg
XM_011533338.1:c.8212G>A XP_011531640.1:p.Gly2738Arg
XM_017005688.1:c.8185G>A XP_016861177.1:p.Gly2729Arg
XR_001740003.1:n.8281G>A
XR_001740004.1:n.8281G>A
XR_001740005.1:n.8281G>A
XR_940369.1:n.8308G>A
XR_940370.1:n.8308G>A
XR_940371.1:n.8308G>A