Canonical Allele Identifier: CA2579771254

Gene: CALM1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.90404508_90404510delinsACG , CM000676.2:g.90404508_90404510delinsACG	GRCh38
NC_000014.8:g.90870852_90870854delinsACG , CM000676.1:g.90870852_90870854delinsACG	GRCh37
NC_000014.7:g.89940605_89940607delinsACG	NCBI36
NG_013338.1:g.12526_12528delinsACG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356978.9:c.415_417delinsACG MANE Select	ENSP00000349467.4:p.Tyr139Thr
ENST00000447653.8:c.307_309delinsACG	ENSP00000403491.4:p.Tyr103Thr
ENST00000659177.1:c.307_309delinsACG	ENSP00000499421.1:p.Tyr103Thr
ENST00000663135.1:c.307_309delinsACG	ENSP00000499498.1:p.Tyr103Thr
ENST00000356978.8:c.415_417delinsACG	ENSP00000349467.4:p.Tyr139Thr
ENST00000447653.7:c.418_420delinsACG	ENSP00000403491.3:p.Tyr140Thr
ENST00000544280.6:c.307_309delinsACG	ENSP00000442853.2:p.Tyr103Thr
ENST00000553422.1:c.287_289delinsACG	ENSP00000450425.1:n.287_289delinsACG
ENST00000553542.5:c.307_309delinsACG	ENSP00000450829.1:p.Tyr103Thr
ENST00000553630.1:c.*56_*58delinsACG	ENSP00000451646.1:n.*56_*58delinsACG
ENST00000553964.5:n.2545_2547delinsACG
ENST00000554296.1:n.467_469delinsACG
ENST00000556721.1:n.341_343delinsACG
ENST00000626705.2:c.217_219delinsACG	ENSP00000486402.1:p.Tyr73Thr
NM_006888.4:c.415_417delinsACG	NP_008819.1:p.Tyr139Thr
XM_006720258.2:c.418_420delinsACG	XP_006720321.1:p.Tyr140Thr
NM_001363669.1:c.307_309delinsACG	NP_001350598.1:p.Tyr103Thr
NM_001363670.1:c.418_420delinsACG	NP_001350599.1:p.Tyr140Thr
NM_006888.5:c.415_417delinsACG	NP_008819.1:p.Tyr139Thr
NM_006888.6:c.415_417delinsACG MANE Select	NP_008819.1:p.Tyr139Thr
NM_001363669.2:c.307_309delinsACG	NP_001350598.1:p.Tyr103Thr
NM_001363670.2:c.418_420delinsACG	NP_001350599.1:p.Tyr140Thr