Canonical Allele Identifier: CA2740092163
Gene: AMER1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3062083
ClinVar RCV Id: RCV003985193

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.64192411del , CM000685.2:g.64192411del GRCh38
NC_000023.10:g.63412291del , CM000685.1:g.63412291del GRCh37
NC_000023.9:g.63329016del NCBI36
NG_021345.1:g.18335del

Transcript Alleles

HGVS Amino-acid Change
ENST00000374869.8:c.877del MANE Select ENSP00000364003.4:p.Val293Ter
ENST00000330258.3:c.877del ENSP00000329117.3:p.Val293Ter
ENST00000374869.7:c.877del ENSP00000364003.3:p.Val293Ter
NM_152424.3:c.877del NP_689637.3:p.Val293Ter
XM_011530858.1:c.877del XP_011529160.1:p.Val293Ter
NM_152424.4:c.877del MANE Select NP_689637.3:p.Val293Ter