Canonical Allele Identifier: CA2579774327
Gene: CALM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.90404691_90404692delinsCG , CM000676.2:g.90404691_90404692delinsCG GRCh38
NC_000014.8:g.90871035_90871036delinsCG , CM000676.1:g.90871035_90871036delinsCG GRCh37
NC_000014.7:g.89940788_89940789delinsCG NCBI36
NG_013338.1:g.12709_12710delinsCG

Transcript Alleles

HGVS Amino-acid change
ENST00000356978.9:c.424_425delinsCG MANE Select ENSP00000349467.4:p.Phe142Arg
ENST00000447653.8:c.316_317delinsCG ENSP00000403491.4:p.Phe106Arg
ENST00000659177.1:c.316_317delinsCG ENSP00000499421.1:p.Phe106Arg
ENST00000663135.1:c.316_317delinsCG ENSP00000499498.1:p.Phe106Arg
ENST00000356978.8:c.424_425delinsCG ENSP00000349467.4:p.Phe142Arg
ENST00000447653.7:c.427_428delinsCG ENSP00000403491.3:p.Phe143Arg
ENST00000544280.6:c.316_317delinsCG ENSP00000442853.2:p.Phe106Arg
ENST00000553422.1:c.296_297delinsCG ENSP00000450425.1:n.296_297delinsCG
ENST00000553542.5:c.316_317delinsCG ENSP00000450829.1:p.Phe106Arg
ENST00000553630.1:c.*65_*66delinsCG ENSP00000451646.1:n.*65_*66delinsCG
ENST00000553964.5:n.2554_2555delinsCG
ENST00000554296.1:n.476_477delinsCG
ENST00000556721.1:n.350_351delinsCG
ENST00000626705.2:c.226_227delinsCG ENSP00000486402.1:p.Phe76Arg
NM_006888.4:c.424_425delinsCG NP_008819.1:p.Phe142Arg
XM_006720258.2:c.427_428delinsCG XP_006720321.1:p.Phe143Arg
NM_001363669.1:c.316_317delinsCG NP_001350598.1:p.Phe106Arg
NM_001363670.1:c.427_428delinsCG NP_001350599.1:p.Phe143Arg
NM_006888.5:c.424_425delinsCG NP_008819.1:p.Phe142Arg
NM_006888.6:c.424_425delinsCG MANE Select NP_008819.1:p.Phe142Arg
NM_001363669.2:c.316_317delinsCG NP_001350598.1:p.Phe106Arg
NM_001363670.2:c.427_428delinsCG NP_001350599.1:p.Phe143Arg