Canonical Allele Identifier: CA390690131
Gene: CALM1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.90404393T>A , CM000676.2:g.90404393T>A GRCh38
NC_000014.8:g.90870737T>A , CM000676.1:g.90870737T>A GRCh37
NC_000014.7:g.89940490T>A NCBI36
NG_013338.1:g.12411T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356978.9:c.300T>A MANE Select ENSP00000349467.4:p.Tyr100Ter
ENST00000447653.8:c.192T>A ENSP00000403491.4:p.Tyr64Ter
ENST00000659177.1:c.192T>A ENSP00000499421.1:p.Tyr64Ter
ENST00000663135.1:c.192T>A ENSP00000499498.1:p.Tyr64Ter
ENST00000356978.8:c.300T>A ENSP00000349467.4:p.Tyr100Ter
ENST00000447653.7:c.303T>A ENSP00000403491.3:p.Tyr101Ter
ENST00000544280.6:c.192T>A ENSP00000442853.2:p.Tyr64Ter
ENST00000553422.1:c.178-6T>A ENSP00000450425.1:n.178-6T>A
ENST00000553542.5:c.192T>A ENSP00000450829.1:p.Tyr64Ter
ENST00000553630.1:c.193T>A ENSP00000451646.1:p.Tyr65Asn
ENST00000553964.5:n.2430T>A
ENST00000554296.1:n.352T>A
ENST00000556721.1:n.226T>A
ENST00000557020.5:c.192T>A ENSP00000451062.1:p.Tyr64Ter
ENST00000626705.2:c.166-64T>A ENSP00000486402.1:n.166-64T>A
NM_006888.4:c.300T>A NP_008819.1:p.Tyr100Ter
XM_006720258.2:c.303T>A XP_006720321.1:p.Tyr101Ter
NM_001363669.1:c.192T>A NP_001350598.1:p.Tyr64Ter
NM_001363670.1:c.303T>A NP_001350599.1:p.Tyr101Ter
NM_006888.5:c.300T>A NP_008819.1:p.Tyr100Ter
NM_006888.6:c.300T>A MANE Select NP_008819.1:p.Tyr100Ter
NM_001363669.2:c.192T>A NP_001350598.1:p.Tyr64Ter
NM_001363670.2:c.303T>A NP_001350599.1:p.Tyr101Ter