Canonical Allele Identifier: CA2433379279
Gene: AMER1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.64192141T= , CM000685.2:g.64192141T= GRCh38
NC_000023.10:g.63412021T= , CM000685.1:g.63412021T= GRCh37
NC_000023.9:g.63328746T= NCBI36
NG_021345.1:g.18604A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374869.8:c.1146A= MANE Select ENSP00000364003.4:p.Glu382=
ENST00000330258.3:c.1146A= ENSP00000329117.3:p.Glu382=
ENST00000374869.7:c.1146A= ENSP00000364003.3:p.Glu382=
NM_152424.3:c.1146A= NP_689637.3:p.Glu382=
XM_011530858.1:c.1146A= XP_011529160.1:p.Glu382=
NM_152424.4:c.1146A= MANE Select NP_689637.3:p.Glu382=