Canonical Allele Identifier: CA390690406

Gene: CALM1

Linked Data

• MyVariant Identifiers: chr14:g.90870853A>T (hg19) ; chr14:g.90404509A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.90404509A>T , CM000676.2:g.90404509A>T	GRCh38
NC_000014.8:g.90870853A>T , CM000676.1:g.90870853A>T	GRCh37
NC_000014.7:g.89940606A>T	NCBI36
NG_013338.1:g.12527A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356978.9:c.416A>T MANE Select	ENSP00000349467.4:p.Tyr139Phe
ENST00000447653.8:c.308A>T	ENSP00000403491.4:p.Tyr103Phe
ENST00000659177.1:c.308A>T	ENSP00000499421.1:p.Tyr103Phe
ENST00000663135.1:c.308A>T	ENSP00000499498.1:p.Tyr103Phe
ENST00000356978.8:c.416A>T	ENSP00000349467.4:p.Tyr139Phe
ENST00000447653.7:c.419A>T	ENSP00000403491.3:p.Tyr140Phe
ENST00000544280.6:c.308A>T	ENSP00000442853.2:p.Tyr103Phe
ENST00000553422.1:c.288A>T	ENSP00000450425.1:n.288A>T
ENST00000553542.5:c.308A>T	ENSP00000450829.1:p.Tyr103Phe
ENST00000553630.1:c.*57A>T	ENSP00000451646.1:n.*57A>T
ENST00000553964.5:n.2546A>T
ENST00000554296.1:n.468A>T
ENST00000556721.1:n.342A>T
ENST00000626705.2:c.218A>T	ENSP00000486402.1:p.Tyr73Phe
NM_006888.4:c.416A>T	NP_008819.1:p.Tyr139Phe
XM_006720258.2:c.419A>T	XP_006720321.1:p.Tyr140Phe
NM_001363669.1:c.308A>T	NP_001350598.1:p.Tyr103Phe
NM_001363670.1:c.419A>T	NP_001350599.1:p.Tyr140Phe
NM_006888.5:c.416A>T	NP_008819.1:p.Tyr139Phe
NM_006888.6:c.416A>T MANE Select	NP_008819.1:p.Tyr139Phe
NM_001363669.2:c.308A>T	NP_001350598.1:p.Tyr103Phe
NM_001363670.2:c.419A>T	NP_001350599.1:p.Tyr140Phe