Canonical Allele Identifier: CA2579771632

Gene: CALM1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.90404380_90404381delinsCC , CM000676.2:g.90404380_90404381delinsCC	GRCh38
NC_000014.8:g.90870724_90870725delinsCC , CM000676.1:g.90870724_90870725delinsCC	GRCh37
NC_000014.7:g.89940477_89940478delinsCC	NCBI36
NG_013338.1:g.12398_12399delinsCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356978.9:c.287_288delinsCC MANE Select	ENSP00000349467.4:p.Asp96Ala
ENST00000447653.8:c.179_180delinsCC	ENSP00000403491.4:p.Asp60Ala
ENST00000659177.1:c.179_180delinsCC	ENSP00000499421.1:p.Asp60Ala
ENST00000663135.1:c.179_180delinsCC	ENSP00000499498.1:p.Asp60Ala
ENST00000356978.8:c.287_288delinsCC	ENSP00000349467.4:p.Asp96Ala
ENST00000447653.7:c.290_291delinsCC	ENSP00000403491.3:p.Asp97Ala
ENST00000544280.6:c.179_180delinsCC	ENSP00000442853.2:p.Asp60Ala
ENST00000553422.1:c.178-19_178-18delinsCC	ENSP00000450425.1:n.178-19_178-18delinsCC
ENST00000553542.5:c.179_180delinsCC	ENSP00000450829.1:p.Asp60Ala
ENST00000553630.1:c.180_181delinsCC	ENSP00000451646.1:p.Trp61Arg
ENST00000553964.5:n.2417_2418delinsCC
ENST00000554296.1:n.339_340delinsCC
ENST00000556721.1:n.213_214delinsCC
ENST00000557020.5:c.179_180delinsCC	ENSP00000451062.1:p.Asp60Ala
ENST00000626705.2:c.166-77_166-76delinsCC	ENSP00000486402.1:n.166-77_166-76delinsCC
NM_006888.4:c.287_288delinsCC	NP_008819.1:p.Asp96Ala
XM_006720258.2:c.290_291delinsCC	XP_006720321.1:p.Asp97Ala
NM_001363669.1:c.179_180delinsCC	NP_001350598.1:p.Asp60Ala
NM_001363670.1:c.290_291delinsCC	NP_001350599.1:p.Asp97Ala
NM_006888.5:c.287_288delinsCC	NP_008819.1:p.Asp96Ala
NM_006888.6:c.287_288delinsCC MANE Select	NP_008819.1:p.Asp96Ala
NM_001363669.2:c.179_180delinsCC	NP_001350598.1:p.Asp60Ala
NM_001363670.2:c.290_291delinsCC	NP_001350599.1:p.Asp97Ala