Canonical Allele Identifier: CA2579770127

Gene: CALM1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.90404382_90404384delinsTTT , CM000676.2:g.90404382_90404384delinsTTT	GRCh38
NC_000014.8:g.90870726_90870728delinsTTT , CM000676.1:g.90870726_90870728delinsTTT	GRCh37
NC_000014.7:g.89940479_89940481delinsTTT	NCBI36
NG_013338.1:g.12400_12402delinsTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356978.9:c.289_291delinsTTT MANE Select	ENSP00000349467.4:p.Gly97Phe
ENST00000447653.8:c.181_183delinsTTT	ENSP00000403491.4:p.Gly61Phe
ENST00000659177.1:c.181_183delinsTTT	ENSP00000499421.1:p.Gly61Phe
ENST00000663135.1:c.181_183delinsTTT	ENSP00000499498.1:p.Gly61Phe
ENST00000356978.8:c.289_291delinsTTT	ENSP00000349467.4:p.Gly97Phe
ENST00000447653.7:c.292_294delinsTTT	ENSP00000403491.3:p.Gly98Phe
ENST00000544280.6:c.181_183delinsTTT	ENSP00000442853.2:p.Gly61Phe
ENST00000553422.1:c.178-17_178-15delinsTTT	ENSP00000450425.1:n.178-17_178-15delinsTTT
ENST00000553542.5:c.181_183delinsTTT	ENSP00000450829.1:p.Gly61Phe
ENST00000553630.1:c.182_184delinsTTT	ENSP00000451646.1:p.Trp61PhefsTer2
ENST00000553964.5:n.2419_2421delinsTTT
ENST00000554296.1:n.341_343delinsTTT
ENST00000556721.1:n.215_217delinsTTT
ENST00000557020.5:c.181_183delinsTTT	ENSP00000451062.1:p.Gly61Phe
ENST00000626705.2:c.166-75_166-73delinsTTT	ENSP00000486402.1:n.166-75_166-73delinsTTT
NM_006888.4:c.289_291delinsTTT	NP_008819.1:p.Gly97Phe
XM_006720258.2:c.292_294delinsTTT	XP_006720321.1:p.Gly98Phe
NM_001363669.1:c.181_183delinsTTT	NP_001350598.1:p.Gly61Phe
NM_001363670.1:c.292_294delinsTTT	NP_001350599.1:p.Gly98Phe
NM_006888.5:c.289_291delinsTTT	NP_008819.1:p.Gly97Phe
NM_006888.6:c.289_291delinsTTT MANE Select	NP_008819.1:p.Gly97Phe
NM_001363669.2:c.181_183delinsTTT	NP_001350598.1:p.Gly61Phe
NM_001363670.2:c.292_294delinsTTT	NP_001350599.1:p.Gly98Phe