Canonical Allele Identifier: CA2579770699
Gene: CALM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.90404509_90404510delinsTG , CM000676.2:g.90404509_90404510delinsTG GRCh38
NC_000014.8:g.90870853_90870854delinsTG , CM000676.1:g.90870853_90870854delinsTG GRCh37
NC_000014.7:g.89940606_89940607delinsTG NCBI36
NG_013338.1:g.12527_12528delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000356978.9:c.416_417delinsTG MANE Select ENSP00000349467.4:p.Tyr139Leu
ENST00000447653.8:c.308_309delinsTG ENSP00000403491.4:p.Tyr103Leu
ENST00000659177.1:c.308_309delinsTG ENSP00000499421.1:p.Tyr103Leu
ENST00000663135.1:c.308_309delinsTG ENSP00000499498.1:p.Tyr103Leu
ENST00000356978.8:c.416_417delinsTG ENSP00000349467.4:p.Tyr139Leu
ENST00000447653.7:c.419_420delinsTG ENSP00000403491.3:p.Tyr140Leu
ENST00000544280.6:c.308_309delinsTG ENSP00000442853.2:p.Tyr103Leu
ENST00000553422.1:c.288_289delinsTG ENSP00000450425.1:n.288_289delinsTG
ENST00000553542.5:c.308_309delinsTG ENSP00000450829.1:p.Tyr103Leu
ENST00000553630.1:c.*57_*58delinsTG ENSP00000451646.1:n.*57_*58delinsTG
ENST00000553964.5:n.2546_2547delinsTG
ENST00000554296.1:n.468_469delinsTG
ENST00000556721.1:n.342_343delinsTG
ENST00000626705.2:c.218_219delinsTG ENSP00000486402.1:p.Tyr73Leu
NM_006888.4:c.416_417delinsTG NP_008819.1:p.Tyr139Leu
XM_006720258.2:c.419_420delinsTG XP_006720321.1:p.Tyr140Leu
NM_001363669.1:c.308_309delinsTG NP_001350598.1:p.Tyr103Leu
NM_001363670.1:c.419_420delinsTG NP_001350599.1:p.Tyr140Leu
NM_006888.5:c.416_417delinsTG NP_008819.1:p.Tyr139Leu
NM_006888.6:c.416_417delinsTG MANE Select NP_008819.1:p.Tyr139Leu
NM_001363669.2:c.308_309delinsTG NP_001350598.1:p.Tyr103Leu
NM_001363670.2:c.419_420delinsTG NP_001350599.1:p.Tyr140Leu