Canonical Allele Identifier: CA413309492
Gene: AMER1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.64192488A>T , CM000685.2:g.64192488A>T GRCh38
NC_000023.10:g.63412368A>T , CM000685.1:g.63412368A>T GRCh37
NC_000023.9:g.63329093A>T NCBI36
NG_021345.1:g.18257T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000374869.8:c.799T>A MANE Select ENSP00000364003.4:p.Ser267Thr
ENST00000330258.3:c.799T>A ENSP00000329117.3:p.Ser267Thr
ENST00000374869.7:c.799T>A ENSP00000364003.3:p.Ser267Thr
NM_152424.3:c.799T>A NP_689637.3:p.Ser267Thr
XM_011530858.1:c.799T>A XP_011529160.1:p.Ser267Thr
NM_152424.4:c.799T>A MANE Select NP_689637.3:p.Ser267Thr