Canonical Allele Identifier: CA2426745290

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949961C= , CM000685.2:g.43949961C= GRCh38
NC_000023.10:g.43809207C= , CM000685.1:g.43809207C= GRCh37
NC_000023.9:g.43694151C= NCBI36
NG_009832.1:g.28715G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000642620.1:c.240G= (NDP) MANE Select ENSP00000495972.1:p.Ser80=
ENST00000647044.1:c.240G= (NDP) ENSP00000495811.1:p.Ser80=
ENST00000378062.5:c.240G= (NDP) ENSP00000367301.5:p.Ser80=
ENST00000470584.1:n.284G= (NDP)
NM_000266.3:c.240G= (NDP) NP_000257.1:p.Ser80=
NR_046631.1:n.230C= (NDP-AS1)
NM_000266.4:c.240G= (NDP) MANE Select NP_000257.1:p.Ser80=