Canonical Allele Identifier: CA487760022

Gene: CALM1

Linked Data

• MyVariant Identifiers: chr14:g.90870731T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.90404387T>C , CM000676.2:g.90404387T>C	GRCh38
NC_000014.8:g.90870731T>C , CM000676.1:g.90870731T>C	GRCh37
NC_000014.7:g.89940484T>C	NCBI36
NG_013338.1:g.12405T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356978.9:c.294T>C MANE Select	ENSP00000349467.4:p.Asn98=
ENST00000447653.8:c.186T>C	ENSP00000403491.4:p.Asn62=
ENST00000659177.1:c.186T>C	ENSP00000499421.1:p.Asn62=
ENST00000663135.1:c.186T>C	ENSP00000499498.1:p.Asn62=
ENST00000356978.8:c.294T>C	ENSP00000349467.4:p.Asn98=
ENST00000447653.7:c.297T>C	ENSP00000403491.3:p.Asn99=
ENST00000544280.6:c.186T>C	ENSP00000442853.2:p.Asn62=
ENST00000553422.1:c.178-12T>C	ENSP00000450425.1:n.178-12T>C
ENST00000553542.5:c.186T>C	ENSP00000450829.1:p.Asn62=
ENST00000553630.1:c.187T>C	ENSP00000451646.1:p.Trp63Arg
ENST00000553964.5:n.2424T>C
ENST00000554296.1:n.346T>C
ENST00000556721.1:n.220T>C
ENST00000557020.5:c.186T>C	ENSP00000451062.1:p.Asn62=
ENST00000626705.2:c.166-70T>C	ENSP00000486402.1:n.166-70T>C
NM_006888.4:c.294T>C	NP_008819.1:p.Asn98=
XM_006720258.2:c.297T>C	XP_006720321.1:p.Asn99=
NM_001363669.1:c.186T>C	NP_001350598.1:p.Asn62=
NM_001363670.1:c.297T>C	NP_001350599.1:p.Asn99=
NM_006888.5:c.294T>C	NP_008819.1:p.Asn98=
NM_006888.6:c.294T>C MANE Select	NP_008819.1:p.Asn98=
NM_001363669.2:c.186T>C	NP_001350598.1:p.Asn62=
NM_001363670.2:c.297T>C	NP_001350599.1:p.Asn99=