Canonical Allele Identifier: CA2579773594

Gene: CALM1

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.90404385_90404387delinsTAG , CM000676.2:g.90404385_90404387delinsTAG	GRCh38
NC_000014.8:g.90870729_90870731delinsTAG , CM000676.1:g.90870729_90870731delinsTAG	GRCh37
NC_000014.7:g.89940482_89940484delinsTAG	NCBI36
NG_013338.1:g.12403_12405delinsTAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356978.9:c.292_294delinsTAG MANE Select	ENSP00000349467.4:p.Asn98Ter
ENST00000447653.8:c.184_186delinsTAG	ENSP00000403491.4:p.Asn62Ter
ENST00000659177.1:c.184_186delinsTAG	ENSP00000499421.1:p.Asn62Ter
ENST00000663135.1:c.184_186delinsTAG	ENSP00000499498.1:p.Asn62Ter
ENST00000356978.8:c.292_294delinsTAG	ENSP00000349467.4:p.Asn98Ter
ENST00000447653.7:c.295_297delinsTAG	ENSP00000403491.3:p.Asn99Ter
ENST00000544280.6:c.184_186delinsTAG	ENSP00000442853.2:p.Asn62Ter
ENST00000553422.1:c.178-14_178-12delinsTAG	ENSP00000450425.1:n.178-14_178-12delinsTAG
ENST00000553542.5:c.184_186delinsTAG	ENSP00000450829.1:p.Asn62Ter
ENST00000553630.1:c.185_187delinsTAG	ENSP00000451646.1:p.Gln62_Trp63delinsLeuGly
ENST00000553964.5:n.2422_2424delinsTAG
ENST00000554296.1:n.344_346delinsTAG
ENST00000556721.1:n.218_220delinsTAG
ENST00000557020.5:c.184_186delinsTAG	ENSP00000451062.1:p.Asn62Ter
ENST00000626705.2:c.166-72_166-70delinsTAG	ENSP00000486402.1:n.166-72_166-70delinsTAG
NM_006888.4:c.292_294delinsTAG	NP_008819.1:p.Asn98Ter
XM_006720258.2:c.295_297delinsTAG	XP_006720321.1:p.Asn99Ter
NM_001363669.1:c.184_186delinsTAG	NP_001350598.1:p.Asn62Ter
NM_001363670.1:c.295_297delinsTAG	NP_001350599.1:p.Asn99Ter
NM_006888.5:c.292_294delinsTAG	NP_008819.1:p.Asn98Ter
NM_006888.6:c.292_294delinsTAG MANE Select	NP_008819.1:p.Asn98Ter
NM_001363669.2:c.184_186delinsTAG	NP_001350598.1:p.Asn62Ter
NM_001363670.2:c.295_297delinsTAG	NP_001350599.1:p.Asn99Ter