Canonical Allele Identifier: CA2154484304
Gene: CALM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.90404598T= , CM000676.2:g.90404598T= GRCh38
NC_000014.8:g.90870942T= , CM000676.1:g.90870942T= GRCh37
NC_000014.7:g.89940695T= NCBI36
NG_013338.1:g.12616T=

Transcript Alleles

HGVS Amino-acid change
ENST00000356978.9:c.421+84T= MANE Select ENSP00000349467.4:n.421+84T=
ENST00000447653.8:c.313+84T= ENSP00000403491.4:n.313+84T=
ENST00000659177.1:c.313+84T= ENSP00000499421.1:n.313+84T=
ENST00000663135.1:c.313+84T= ENSP00000499498.1:n.313+84T=
ENST00000356978.8:c.421+84T= ENSP00000349467.4:n.421+84T=
ENST00000447653.7:c.424+84T= ENSP00000403491.3:n.424+84T=
ENST00000544280.6:c.313+84T= ENSP00000442853.2:n.313+84T=
ENST00000553422.1:c.293+84T= ENSP00000450425.1:n.293+84T=
ENST00000553542.5:c.313+84T= ENSP00000450829.1:n.313+84T=
ENST00000553630.1:c.*62+84T= ENSP00000451646.1:n.*62+84T=
ENST00000553964.5:n.2551+84T=
ENST00000554296.1:n.473+84T=
ENST00000556721.1:n.347+84T=
ENST00000626705.2:c.223+84T= ENSP00000486402.1:n.223+84T=
NM_006888.4:c.421+84T= NP_008819.1:n.421+84T=
XM_006720258.2:c.424+84T= XP_006720321.1:n.424+84T=
NM_001363669.1:c.313+84T= NP_001350598.1:n.313+84T=
NM_001363670.1:c.424+84T= NP_001350599.1:n.424+84T=
NM_006888.5:c.421+84T= NP_008819.1:n.421+84T=
NM_006888.6:c.421+84T= MANE Select NP_008819.1:n.421+84T=
NM_001363669.2:c.313+84T= NP_001350598.1:n.313+84T=
NM_001363670.2:c.424+84T= NP_001350599.1:n.424+84T=