Canonical Allele Identifier: CA413309672
Gene: AMER1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.63412406G>T (hg19) chrX:g.64192526G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.64192526G>T , CM000685.2:g.64192526G>T GRCh38
NC_000023.10:g.63412406G>T , CM000685.1:g.63412406G>T GRCh37
NC_000023.9:g.63329131G>T NCBI36
NG_021345.1:g.18219C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000374869.8:c.761C>A MANE Select ENSP00000364003.4:p.Ala254Asp
ENST00000330258.3:c.761C>A ENSP00000329117.3:p.Ala254Asp
ENST00000374869.7:c.761C>A ENSP00000364003.3:p.Ala254Asp
NM_152424.3:c.761C>A NP_689637.3:p.Ala254Asp
XM_011530858.1:c.761C>A XP_011529160.1:p.Ala254Asp
NM_152424.4:c.761C>A MANE Select NP_689637.3:p.Ala254Asp
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