Canonical Allele Identifier: CA2579770987

Gene: CALM1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.90404508_90404509delinsGG , CM000676.2:g.90404508_90404509delinsGG	GRCh38
NC_000014.8:g.90870852_90870853delinsGG , CM000676.1:g.90870852_90870853delinsGG	GRCh37
NC_000014.7:g.89940605_89940606delinsGG	NCBI36
NG_013338.1:g.12526_12527delinsGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356978.9:c.415_416delinsGG MANE Select	ENSP00000349467.4:p.Tyr139Gly
ENST00000447653.8:c.307_308delinsGG	ENSP00000403491.4:p.Tyr103Gly
ENST00000659177.1:c.307_308delinsGG	ENSP00000499421.1:p.Tyr103Gly
ENST00000663135.1:c.307_308delinsGG	ENSP00000499498.1:p.Tyr103Gly
ENST00000356978.8:c.415_416delinsGG	ENSP00000349467.4:p.Tyr139Gly
ENST00000447653.7:c.418_419delinsGG	ENSP00000403491.3:p.Tyr140Gly
ENST00000544280.6:c.307_308delinsGG	ENSP00000442853.2:p.Tyr103Gly
ENST00000553422.1:c.287_288delinsGG	ENSP00000450425.1:n.287_288delinsGG
ENST00000553542.5:c.307_308delinsGG	ENSP00000450829.1:p.Tyr103Gly
ENST00000553630.1:c.*56_*57delinsGG	ENSP00000451646.1:n.*56_*57delinsGG
ENST00000553964.5:n.2545_2546delinsGG
ENST00000554296.1:n.467_468delinsGG
ENST00000556721.1:n.341_342delinsGG
ENST00000626705.2:c.217_218delinsGG	ENSP00000486402.1:p.Tyr73Gly
NM_006888.4:c.415_416delinsGG	NP_008819.1:p.Tyr139Gly
XM_006720258.2:c.418_419delinsGG	XP_006720321.1:p.Tyr140Gly
NM_001363669.1:c.307_308delinsGG	NP_001350598.1:p.Tyr103Gly
NM_001363670.1:c.418_419delinsGG	NP_001350599.1:p.Tyr140Gly
NM_006888.5:c.415_416delinsGG	NP_008819.1:p.Tyr139Gly
NM_006888.6:c.415_416delinsGG MANE Select	NP_008819.1:p.Tyr139Gly
NM_001363669.2:c.307_308delinsGG	NP_001350598.1:p.Tyr103Gly
NM_001363670.2:c.418_419delinsGG	NP_001350599.1:p.Tyr140Gly