Canonical Allele Identifier: CA390690111

Gene: CALM1

Linked Data

• MyVariant Identifiers: chr14:g.90870727G>T (hg19) ; chr14:g.90404383G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.90404383G>T , CM000676.2:g.90404383G>T	GRCh38
NC_000014.8:g.90870727G>T , CM000676.1:g.90870727G>T	GRCh37
NC_000014.7:g.89940480G>T	NCBI36
NG_013338.1:g.12401G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356978.9:c.290G>T MANE Select	ENSP00000349467.4:p.Gly97Val
ENST00000447653.8:c.182G>T	ENSP00000403491.4:p.Gly61Val
ENST00000659177.1:c.182G>T	ENSP00000499421.1:p.Gly61Val
ENST00000663135.1:c.182G>T	ENSP00000499498.1:p.Gly61Val
ENST00000356978.8:c.290G>T	ENSP00000349467.4:p.Gly97Val
ENST00000447653.7:c.293G>T	ENSP00000403491.3:p.Gly98Val
ENST00000544280.6:c.182G>T	ENSP00000442853.2:p.Gly61Val
ENST00000553422.1:c.178-16G>T	ENSP00000450425.1:n.178-16G>T
ENST00000553542.5:c.182G>T	ENSP00000450829.1:p.Gly61Val
ENST00000553630.1:c.183G>T	ENSP00000451646.1:p.Trp61Cys
ENST00000553964.5:n.2420G>T
ENST00000554296.1:n.342G>T
ENST00000556721.1:n.216G>T
ENST00000557020.5:c.182G>T	ENSP00000451062.1:p.Gly61Val
ENST00000626705.2:c.166-74G>T	ENSP00000486402.1:n.166-74G>T
NM_006888.4:c.290G>T	NP_008819.1:p.Gly97Val
XM_006720258.2:c.293G>T	XP_006720321.1:p.Gly98Val
NM_001363669.1:c.182G>T	NP_001350598.1:p.Gly61Val
NM_001363670.1:c.293G>T	NP_001350599.1:p.Gly98Val
NM_006888.5:c.290G>T	NP_008819.1:p.Gly97Val
NM_006888.6:c.290G>T MANE Select	NP_008819.1:p.Gly97Val
NM_001363669.2:c.182G>T	NP_001350598.1:p.Gly61Val
NM_001363670.2:c.293G>T	NP_001350599.1:p.Gly98Val