Canonical Allele Identifier: CA2579772647
Gene: CALM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.90404692_90404693delinsGG , CM000676.2:g.90404692_90404693delinsGG GRCh38
NC_000014.8:g.90871036_90871037delinsGG , CM000676.1:g.90871036_90871037delinsGG GRCh37
NC_000014.7:g.89940789_89940790delinsGG NCBI36
NG_013338.1:g.12710_12711delinsGG

Transcript Alleles

HGVS Amino-acid change
ENST00000356978.9:c.425_426delinsGG MANE Select ENSP00000349467.4:p.Phe142Trp
ENST00000447653.8:c.317_318delinsGG ENSP00000403491.4:p.Phe106Trp
ENST00000659177.1:c.317_318delinsGG ENSP00000499421.1:p.Phe106Trp
ENST00000663135.1:c.317_318delinsGG ENSP00000499498.1:p.Phe106Trp
ENST00000356978.8:c.425_426delinsGG ENSP00000349467.4:p.Phe142Trp
ENST00000447653.7:c.428_429delinsGG ENSP00000403491.3:p.Phe143Trp
ENST00000544280.6:c.317_318delinsGG ENSP00000442853.2:p.Phe106Trp
ENST00000553422.1:c.297_298delinsGG ENSP00000450425.1:n.297_298delinsGG
ENST00000553542.5:c.317_318delinsGG ENSP00000450829.1:p.Phe106Trp
ENST00000553630.1:c.*66_*67delinsGG ENSP00000451646.1:n.*66_*67delinsGG
ENST00000553964.5:n.2555_2556delinsGG
ENST00000554296.1:n.477_478delinsGG
ENST00000556721.1:n.351_352delinsGG
ENST00000626705.2:c.227_228delinsGG ENSP00000486402.1:p.Phe76Trp
NM_006888.4:c.425_426delinsGG NP_008819.1:p.Phe142Trp
XM_006720258.2:c.428_429delinsGG XP_006720321.1:p.Phe143Trp
NM_001363669.1:c.317_318delinsGG NP_001350598.1:p.Phe106Trp
NM_001363670.1:c.428_429delinsGG NP_001350599.1:p.Phe143Trp
NM_006888.5:c.425_426delinsGG NP_008819.1:p.Phe142Trp
NM_006888.6:c.425_426delinsGG MANE Select NP_008819.1:p.Phe142Trp
NM_001363669.2:c.317_318delinsGG NP_001350598.1:p.Phe106Trp
NM_001363670.2:c.428_429delinsGG NP_001350599.1:p.Phe143Trp