Canonical Allele Identifier: CA2579770790
Gene: CALM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.90404482_90404483delinsGA , CM000676.2:g.90404482_90404483delinsGA GRCh38
NC_000014.8:g.90870826_90870827delinsGA , CM000676.1:g.90870826_90870827delinsGA GRCh37
NC_000014.7:g.89940579_89940580delinsGA NCBI36
NG_013338.1:g.12500_12501delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000356978.9:c.389_390delinsGA MANE Select ENSP00000349467.4:p.Asp130Gly
ENST00000447653.8:c.281_282delinsGA ENSP00000403491.4:p.Asp94Gly
ENST00000659177.1:c.281_282delinsGA ENSP00000499421.1:p.Asp94Gly
ENST00000663135.1:c.281_282delinsGA ENSP00000499498.1:p.Asp94Gly
ENST00000356978.8:c.389_390delinsGA ENSP00000349467.4:p.Asp130Gly
ENST00000447653.7:c.392_393delinsGA ENSP00000403491.3:p.Asp131Gly
ENST00000544280.6:c.281_282delinsGA ENSP00000442853.2:p.Asp94Gly
ENST00000553422.1:c.261_262delinsGA ENSP00000450425.1:n.261_262delinsGA
ENST00000553542.5:c.281_282delinsGA ENSP00000450829.1:p.Asp94Gly
ENST00000553630.1:c.*30_*31delinsGA ENSP00000451646.1:n.*30_*31delinsGA
ENST00000553964.5:n.2519_2520delinsGA
ENST00000554296.1:n.441_442delinsGA
ENST00000556721.1:n.315_316delinsGA
ENST00000557020.5:c.281_282delinsGA ENSP00000451062.1:p.Asp94Gly
ENST00000626705.2:c.191_192delinsGA ENSP00000486402.1:p.Asp64Gly
NM_006888.4:c.389_390delinsGA NP_008819.1:p.Asp130Gly
XM_006720258.2:c.392_393delinsGA XP_006720321.1:p.Asp131Gly
NM_001363669.1:c.281_282delinsGA NP_001350598.1:p.Asp94Gly
NM_001363670.1:c.392_393delinsGA NP_001350599.1:p.Asp131Gly
NM_006888.5:c.389_390delinsGA NP_008819.1:p.Asp130Gly
NM_006888.6:c.389_390delinsGA MANE Select NP_008819.1:p.Asp130Gly
NM_001363669.2:c.281_282delinsGA NP_001350598.1:p.Asp94Gly
NM_001363670.2:c.392_393delinsGA NP_001350599.1:p.Asp131Gly