Canonical Allele Identifier: CA2579771490
Gene: CALM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.90404379_90404381delinsAGG , CM000676.2:g.90404379_90404381delinsAGG GRCh38
NC_000014.8:g.90870723_90870725delinsAGG , CM000676.1:g.90870723_90870725delinsAGG GRCh37
NC_000014.7:g.89940476_89940478delinsAGG NCBI36
NG_013338.1:g.12397_12399delinsAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000356978.9:c.286_288delinsAGG MANE Select ENSP00000349467.4:p.Asp96Arg
ENST00000447653.8:c.178_180delinsAGG ENSP00000403491.4:p.Asp60Arg
ENST00000659177.1:c.178_180delinsAGG ENSP00000499421.1:p.Asp60Arg
ENST00000663135.1:c.178_180delinsAGG ENSP00000499498.1:p.Asp60Arg
ENST00000356978.8:c.286_288delinsAGG ENSP00000349467.4:p.Asp96Arg
ENST00000447653.7:c.289_291delinsAGG ENSP00000403491.3:p.Asp97Arg
ENST00000544280.6:c.178_180delinsAGG ENSP00000442853.2:p.Asp60Arg
ENST00000553422.1:c.178-20_178-18delinsAGG ENSP00000450425.1:n.178-20_178-18delinsAGG
ENST00000553542.5:c.178_180delinsAGG ENSP00000450829.1:p.Asp60Arg
ENST00000553630.1:c.179_181delinsAGG ENSP00000451646.1:p.Gly60_Trp61delinsGluGly
ENST00000553964.5:n.2416_2418delinsAGG
ENST00000554296.1:n.338_340delinsAGG
ENST00000556721.1:n.212_214delinsAGG
ENST00000557020.5:c.178_180delinsAGG ENSP00000451062.1:p.Asp60Arg
ENST00000626705.2:c.166-78_166-76delinsAGG ENSP00000486402.1:n.166-78_166-76delinsAGG
NM_006888.4:c.286_288delinsAGG NP_008819.1:p.Asp96Arg
XM_006720258.2:c.289_291delinsAGG XP_006720321.1:p.Asp97Arg
NM_001363669.1:c.178_180delinsAGG NP_001350598.1:p.Asp60Arg
NM_001363670.1:c.289_291delinsAGG NP_001350599.1:p.Asp97Arg
NM_006888.5:c.286_288delinsAGG NP_008819.1:p.Asp96Arg
NM_006888.6:c.286_288delinsAGG MANE Select NP_008819.1:p.Asp96Arg
NM_001363669.2:c.178_180delinsAGG NP_001350598.1:p.Asp60Arg
NM_001363670.2:c.289_291delinsAGG NP_001350599.1:p.Asp97Arg