Canonical Allele Identifier: CA2433379216
Gene: AMER1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.64191990G= , CM000685.2:g.64191990G= GRCh38
NC_000023.10:g.63411870G= , CM000685.1:g.63411870G= GRCh37
NC_000023.9:g.63328595G= NCBI36
NG_021345.1:g.18755C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374869.8:c.1297C= MANE Select ENSP00000364003.4:p.His433=
ENST00000330258.3:c.1297C= ENSP00000329117.3:p.His433=
ENST00000374869.7:c.1297C= ENSP00000364003.3:p.His433=
NM_152424.3:c.1297C= NP_689637.3:p.His433=
XM_011530858.1:c.1297C= XP_011529160.1:p.His433=
NM_152424.4:c.1297C= MANE Select NP_689637.3:p.His433=