Canonical Allele Identifier: CA2579774132
Gene: CALM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.90404385_90404386delinsTG , CM000676.2:g.90404385_90404386delinsTG GRCh38
NC_000014.8:g.90870729_90870730delinsTG , CM000676.1:g.90870729_90870730delinsTG GRCh37
NC_000014.7:g.89940482_89940483delinsTG NCBI36
NG_013338.1:g.12403_12404delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000356978.9:c.292_293delinsTG MANE Select ENSP00000349467.4:p.Asn98Cys
ENST00000447653.8:c.184_185delinsTG ENSP00000403491.4:p.Asn62Cys
ENST00000659177.1:c.184_185delinsTG ENSP00000499421.1:p.Asn62Cys
ENST00000663135.1:c.184_185delinsTG ENSP00000499498.1:p.Asn62Cys
ENST00000356978.8:c.292_293delinsTG ENSP00000349467.4:p.Asn98Cys
ENST00000447653.7:c.295_296delinsTG ENSP00000403491.3:p.Asn99Cys
ENST00000544280.6:c.184_185delinsTG ENSP00000442853.2:p.Asn62Cys
ENST00000553422.1:c.178-14_178-13delinsTG ENSP00000450425.1:n.178-14_178-13delinsTG
ENST00000553542.5:c.184_185delinsTG ENSP00000450829.1:p.Asn62Cys
ENST00000553630.1:c.185_186delinsTG ENSP00000451646.1:p.Gln62Leu
ENST00000553964.5:n.2422_2423delinsTG
ENST00000554296.1:n.344_345delinsTG
ENST00000556721.1:n.218_219delinsTG
ENST00000557020.5:c.184_185delinsTG ENSP00000451062.1:p.Asn62Cys
ENST00000626705.2:c.166-72_166-71delinsTG ENSP00000486402.1:n.166-72_166-71delinsTG
NM_006888.4:c.292_293delinsTG NP_008819.1:p.Asn98Cys
XM_006720258.2:c.295_296delinsTG XP_006720321.1:p.Asn99Cys
NM_001363669.1:c.184_185delinsTG NP_001350598.1:p.Asn62Cys
NM_001363670.1:c.295_296delinsTG NP_001350599.1:p.Asn99Cys
NM_006888.5:c.292_293delinsTG NP_008819.1:p.Asn98Cys
NM_006888.6:c.292_293delinsTG MANE Select NP_008819.1:p.Asn98Cys
NM_001363669.2:c.184_185delinsTG NP_001350598.1:p.Asn62Cys
NM_001363670.2:c.295_296delinsTG NP_001350599.1:p.Asn99Cys