Canonical Allele Identifier: CA2433379348
Gene: AMER1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.64192351C= , CM000685.2:g.64192351C= GRCh38
NC_000023.10:g.63412231C= , CM000685.1:g.63412231C= GRCh37
NC_000023.9:g.63328956C= NCBI36
NG_021345.1:g.18394G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374869.8:c.936G= MANE Select ENSP00000364003.4:p.Leu312=
ENST00000330258.3:c.936G= ENSP00000329117.3:p.Leu312=
ENST00000374869.7:c.936G= ENSP00000364003.3:p.Leu312=
NM_152424.3:c.936G= NP_689637.3:p.Leu312=
XM_011530858.1:c.936G= XP_011529160.1:p.Leu312=
NM_152424.4:c.936G= MANE Select NP_689637.3:p.Leu312=