Canonical Allele Identifier: CA2426748413

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43958357A= , CM000685.2:g.43958357A= GRCh38
NC_000023.10:g.43817603A= , CM000685.1:g.43817603A= GRCh37
NC_000023.9:g.43702547A= NCBI36
NG_009832.1:g.20319T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000642620.1:c.174+115T= (NDP) MANE Select ENSP00000495972.1:n.174+115T=
ENST00000647044.1:c.174+115T= (NDP) ENSP00000495811.1:n.174+115T=
ENST00000378062.5:c.174+115T= (NDP) ENSP00000367301.5:n.174+115T=
ENST00000470584.1:n.218+361T= (NDP)
NM_000266.3:c.174+115T= (NDP) NP_000257.1:n.174+115T=
NR_046631.1:n.467-2428A= (NDP-AS1)
NM_000266.4:c.174+115T= (NDP) MANE Select NP_000257.1:n.174+115T=