Canonical Allele Identifier: CA2433379213
Gene: AMER1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.64191985G= , CM000685.2:g.64191985G= GRCh38
NC_000023.10:g.63411865G= , CM000685.1:g.63411865G= GRCh37
NC_000023.9:g.63328590G= NCBI36
NG_021345.1:g.18760C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374869.8:c.1302C= MANE Select ENSP00000364003.4:p.His434=
ENST00000330258.3:c.1302C= ENSP00000329117.3:p.His434=
ENST00000374869.7:c.1302C= ENSP00000364003.3:p.His434=
NM_152424.3:c.1302C= NP_689637.3:p.His434=
XM_011530858.1:c.1302C= XP_011529160.1:p.His434=
NM_152424.4:c.1302C= MANE Select NP_689637.3:p.His434=
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