Canonical Allele Identifier: CA2433379239
Gene: AMER1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.64192045T= , CM000685.2:g.64192045T= GRCh38
NC_000023.10:g.63411925T= , CM000685.1:g.63411925T= GRCh37
NC_000023.9:g.63328650T= NCBI36
NG_021345.1:g.18700A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374869.8:c.1242A= MANE Select ENSP00000364003.4:p.Gln414=
ENST00000330258.3:c.1242A= ENSP00000329117.3:p.Gln414=
ENST00000374869.7:c.1242A= ENSP00000364003.3:p.Gln414=
NM_152424.3:c.1242A= NP_689637.3:p.Gln414=
XM_011530858.1:c.1242A= XP_011529160.1:p.Gln414=
NM_152424.4:c.1242A= MANE Select NP_689637.3:p.Gln414=