Canonical Allele Identifier: CA913191003
Gene: AMER1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.64192521dup , CM000685.2:g.64192521dup GRCh38
NC_000023.10:g.63412401dup , CM000685.1:g.63412401dup GRCh37
NC_000023.9:g.63329126dup NCBI36
NG_021345.1:g.18226dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000374869.8:c.768dup MANE Select ENSP00000364003.4:p.Asp257ArgfsTer21
ENST00000330258.3:c.768dup ENSP00000329117.3:p.Asp257ArgfsTer21
ENST00000374869.7:c.768dup ENSP00000364003.3:p.Asp257ArgfsTer21
NM_152424.3:c.768dup NP_689637.3:p.Asp257ArgfsTer21
XM_011530858.1:c.768dup XP_011529160.1:p.Asp257ArgfsTer21
NM_152424.4:c.768dup MANE Select NP_689637.3:p.Asp257ArgfsTer21