Canonical Allele Identifier: CA2579771368

Gene: CALM1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.90404395_90404396delinsGT , CM000676.2:g.90404395_90404396delinsGT	GRCh38
NC_000014.8:g.90870739_90870740delinsGT , CM000676.1:g.90870739_90870740delinsGT	GRCh37
NC_000014.7:g.89940492_89940493delinsGT	NCBI36
NG_013338.1:g.12413_12414delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356978.9:c.302_303delinsGT MANE Select	ENSP00000349467.4:p.Ile101Ser
ENST00000447653.8:c.194_195delinsGT	ENSP00000403491.4:p.Ile65Ser
ENST00000659177.1:c.194_195delinsGT	ENSP00000499421.1:p.Ile65Ser
ENST00000663135.1:c.194_195delinsGT	ENSP00000499498.1:p.Ile65Ser
ENST00000356978.8:c.302_303delinsGT	ENSP00000349467.4:p.Ile101Ser
ENST00000447653.7:c.305_306delinsGT	ENSP00000403491.3:p.Ile102Ser
ENST00000544280.6:c.194_195delinsGT	ENSP00000442853.2:p.Ile65Ser
ENST00000553422.1:c.178-4_178-3delinsGT	ENSP00000450425.1:n.178-4_178-3delinsGT
ENST00000553542.5:c.194_195delinsGT	ENSP00000450829.1:p.Ile65Ser
ENST00000553630.1:c.195_196delinsGT	ENSP00000451646.1:p.Tyr65Ter
ENST00000553964.5:n.2432_2433delinsGT
ENST00000554296.1:n.354_355delinsGT
ENST00000556721.1:n.228_229delinsGT
ENST00000557020.5:c.194_195delinsGT	ENSP00000451062.1:p.Ile65Ser
ENST00000626705.2:c.166-62_166-61delinsGT	ENSP00000486402.1:n.166-62_166-61delinsGT
NM_006888.4:c.302_303delinsGT	NP_008819.1:p.Ile101Ser
XM_006720258.2:c.305_306delinsGT	XP_006720321.1:p.Ile102Ser
NM_001363669.1:c.194_195delinsGT	NP_001350598.1:p.Ile65Ser
NM_001363670.1:c.305_306delinsGT	NP_001350599.1:p.Ile102Ser
NM_006888.5:c.302_303delinsGT	NP_008819.1:p.Ile101Ser
NM_006888.6:c.302_303delinsGT MANE Select	NP_008819.1:p.Ile101Ser
NM_001363669.2:c.194_195delinsGT	NP_001350598.1:p.Ile65Ser
NM_001363670.2:c.305_306delinsGT	NP_001350599.1:p.Ile102Ser