Canonical Allele Identifier: CA487760030

Gene: CALM1

Linked Data

• MyVariant Identifiers: chr14:g.90870734T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.90404390T>G , CM000676.2:g.90404390T>G	GRCh38
NC_000014.8:g.90870734T>G , CM000676.1:g.90870734T>G	GRCh37
NC_000014.7:g.89940487T>G	NCBI36
NG_013338.1:g.12408T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356978.9:c.297T>G MANE Select	ENSP00000349467.4:p.Gly99=
ENST00000447653.8:c.189T>G	ENSP00000403491.4:p.Gly63=
ENST00000659177.1:c.189T>G	ENSP00000499421.1:p.Gly63=
ENST00000663135.1:c.189T>G	ENSP00000499498.1:p.Gly63=
ENST00000356978.8:c.297T>G	ENSP00000349467.4:p.Gly99=
ENST00000447653.7:c.300T>G	ENSP00000403491.3:p.Gly100=
ENST00000544280.6:c.189T>G	ENSP00000442853.2:p.Gly63=
ENST00000553422.1:c.178-9T>G	ENSP00000450425.1:n.178-9T>G
ENST00000553542.5:c.189T>G	ENSP00000450829.1:p.Gly63=
ENST00000553630.1:c.190T>G	ENSP00000451646.1:p.Leu64Val
ENST00000553964.5:n.2427T>G
ENST00000554296.1:n.349T>G
ENST00000556721.1:n.223T>G
ENST00000557020.5:c.189T>G	ENSP00000451062.1:p.Gly63=
ENST00000626705.2:c.166-67T>G	ENSP00000486402.1:n.166-67T>G
NM_006888.4:c.297T>G	NP_008819.1:p.Gly99=
XM_006720258.2:c.300T>G	XP_006720321.1:p.Gly100=
NM_001363669.1:c.189T>G	NP_001350598.1:p.Gly63=
NM_001363670.1:c.300T>G	NP_001350599.1:p.Gly100=
NM_006888.5:c.297T>G	NP_008819.1:p.Gly99=
NM_006888.6:c.297T>G MANE Select	NP_008819.1:p.Gly99=
NM_001363669.2:c.189T>G	NP_001350598.1:p.Gly63=
NM_001363670.2:c.300T>G	NP_001350599.1:p.Gly100=