Canonical Allele Identifier: CA487760088

Gene: CALM1

Linked Data

• MyVariant Identifiers: chr14:g.90870749A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.90404405A>T , CM000676.2:g.90404405A>T	GRCh38
NC_000014.8:g.90870749A>T , CM000676.1:g.90870749A>T	GRCh37
NC_000014.7:g.89940502A>T	NCBI36
NG_013338.1:g.12423A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356978.9:c.312A>T MANE Select	ENSP00000349467.4:p.Ala104=
ENST00000447653.8:c.204A>T	ENSP00000403491.4:p.Ala68=
ENST00000659177.1:c.204A>T	ENSP00000499421.1:p.Ala68=
ENST00000663135.1:c.204A>T	ENSP00000499498.1:p.Ala68=
ENST00000356978.8:c.312A>T	ENSP00000349467.4:p.Ala104=
ENST00000447653.7:c.315A>T	ENSP00000403491.3:p.Ala105=
ENST00000544280.6:c.204A>T	ENSP00000442853.2:p.Ala68=
ENST00000553422.1:c.184A>T	ENSP00000450425.1:p.Arg62Ter
ENST00000553542.5:c.204A>T	ENSP00000450829.1:p.Ala68=
ENST00000553630.1:c.205A>T	ENSP00000451646.1:p.Arg69Ter
ENST00000553964.5:n.2442A>T
ENST00000554296.1:n.364A>T
ENST00000556721.1:n.238A>T
ENST00000557020.5:c.204A>T	ENSP00000451062.1:p.Ala68=
ENST00000626705.2:c.166-52A>T	ENSP00000486402.1:n.166-52A>T
NM_006888.4:c.312A>T	NP_008819.1:p.Ala104=
XM_006720258.2:c.315A>T	XP_006720321.1:p.Ala105=
NM_001363669.1:c.204A>T	NP_001350598.1:p.Ala68=
NM_001363670.1:c.315A>T	NP_001350599.1:p.Ala105=
NM_006888.5:c.312A>T	NP_008819.1:p.Ala104=
NM_006888.6:c.312A>T MANE Select	NP_008819.1:p.Ala104=
NM_001363669.2:c.204A>T	NP_001350598.1:p.Ala68=
NM_001363670.2:c.315A>T	NP_001350599.1:p.Ala105=