Canonical Allele Identifier: CA2821494683
Gene: AMER1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.64192018del , CM000685.2:g.64192018del GRCh38
NC_000023.10:g.63411898del , CM000685.1:g.63411898del GRCh37
NC_000023.9:g.63328623del NCBI36
NG_021345.1:g.18729del

Transcript Alleles

HGVS Amino-acid Change
ENST00000374869.8:c.1271del MANE Select ENSP00000364003.4:p.Gly424AlafsTer25
ENST00000330258.3:c.1271del ENSP00000329117.3:p.Gly424AlafsTer25
ENST00000374869.7:c.1271del ENSP00000364003.3:p.Gly424AlafsTer25
NM_152424.3:c.1271del NP_689637.3:p.Gly424AlafsTer25
XM_011530858.1:c.1271del XP_011529160.1:p.Gly424AlafsTer25
NM_152424.4:c.1271del MANE Select NP_689637.3:p.Gly424AlafsTer25
Search 100 bp 5'
Search 100 bp 3'