Canonical Allele Identifier: CA339395680
Community Standard Title: NM_005202.4(COL8A2):c.1280G>T (p.Gly427Val)
Gene: COL8A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.36098401C>A , CM000663.2:g.36098401C>A GRCh38
NC_000001.10:g.36564002C>A , CM000663.1:g.36564002C>A GRCh37
NC_000001.9:g.36336589C>A NCBI36
NG_016245.2:g.31684G>T

Transcript Alleles

HGVS Amino-acid Change
NM_005202.4:c.1280G>T MANE Select NP_005193.1:p.Gly427Val
ENST00000397799.2:c.1280G>T MANE Select ENSP00000380901.1:p.Gly427Val
NM_001294347.1:c.1085G>T NP_001281276.1:p.Gly362Val
NM_001294347.2:c.1085G>T NP_001281276.1:p.Gly362Val
NM_005202.3:c.1280G>T NP_005193.1:p.Gly427Val
ENST00000303143.9:c.1280G>T ENSP00000305913.4:p.Gly427Val
ENST00000397799.1:c.1280G>T ENSP00000380901.1:p.Gly427Val
ENST00000481785.1:c.1085G>T ENSP00000436433.1:p.Gly362Val
ENST00000615990.1:c.773-321G>T ENSP00000484406.1:n.773-321G>T
XM_005270477.2:c.1511G>T XP_005270534.1:p.Gly504Val
XM_005270477.3:c.1511G>T XP_005270534.1:p.Gly504Val