Canonical Allele Identifier: CA2433379371
Gene: AMER1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.64192416C= , CM000685.2:g.64192416C= GRCh38
NC_000023.10:g.63412296C= , CM000685.1:g.63412296C= GRCh37
NC_000023.9:g.63329021C= NCBI36
NG_021345.1:g.18329G=

Transcript Alleles

HGVS Amino-acid change
ENST00000374869.8:c.871G= MANE Select ENSP00000364003.4:p.Glu291=
ENST00000330258.3:c.871G= ENSP00000329117.3:p.Glu291=
ENST00000374869.7:c.871G= ENSP00000364003.3:p.Glu291=
NM_152424.3:c.871G= NP_689637.3:p.Glu291=
XM_011530858.1:c.871G= XP_011529160.1:p.Glu291=
NM_152424.4:c.871G= MANE Select NP_689637.3:p.Glu291=