Canonical Allele Identifier: CA367212680
Community Standard Title: NM_018685.5(ANLN):c.1979A>G (p.Asp660Gly)
Gene: ANLN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.36420278A>G , CM000669.2:g.36420278A>G GRCh38
NC_000007.13:g.36459887A>G , CM000669.1:g.36459887A>G GRCh37
NC_000007.12:g.36426412A>G NCBI36
NG_041770.1:g.35476A>G

Transcript Alleles

HGVS Amino-acid Change
NM_018685.5:c.1979A>G MANE Select NP_061155.2:p.Asp660Gly
ENST00000265748.7:c.1979A>G MANE Select ENSP00000265748.2:p.Asp660Gly
NM_001284301.2:c.1868A>G NP_001271230.1:p.Asp623Gly
NM_001284301.3:c.1868A>G NP_001271230.1:p.Asp623Gly
NM_001284302.2:c.1865A>G NP_001271231.1:p.Asp622Gly
NM_001284302.3:c.1865A>G NP_001271231.1:p.Asp622Gly
NM_018685.4:c.1979A>G NP_061155.2:p.Asp660Gly
ENST00000265748.6:c.1979A>G ENSP00000265748.2:p.Asp660Gly
ENST00000396068.6:c.1868A>G ENSP00000379380.2:p.Asp623Gly
ENST00000428612.5:c.97-4267A>G
ENST00000446635.5:c.55A>G
XM_006715746.1:c.1979A>G XP_006715809.1:p.Asp660Gly
XM_006715746.2:c.1979A>G XP_006715809.1:p.Asp660Gly
XM_006715747.2:c.1868A>G XP_006715810.1:p.Asp623Gly
XM_006715747.4:c.1868A>G XP_006715810.1:p.Asp623Gly
XM_017012354.2:c.1967A>G XP_016867843.1:p.Asp656Gly
XM_017012355.2:c.1967A>G XP_016867844.1:p.Asp656Gly
XM_017012356.2:c.1856A>G XP_016867845.1:p.Asp619Gly