Canonical Allele Identifier: CA2433379222
Gene: AMER1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.64192009A= , CM000685.2:g.64192009A= GRCh38
NC_000023.10:g.63411889A= , CM000685.1:g.63411889A= GRCh37
NC_000023.9:g.63328614A= NCBI36
NG_021345.1:g.18736T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374869.8:c.1278T= MANE Select ENSP00000364003.4:p.His426=
ENST00000330258.3:c.1278T= ENSP00000329117.3:p.His426=
ENST00000374869.7:c.1278T= ENSP00000364003.3:p.His426=
NM_152424.3:c.1278T= NP_689637.3:p.His426=
XM_011530858.1:c.1278T= XP_011529160.1:p.His426=
NM_152424.4:c.1278T= MANE Select NP_689637.3:p.His426=
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