Canonical Allele Identifier: CA2426745225

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949783C= , CM000685.2:g.43949783C= GRCh38
NC_000023.10:g.43809029C= , CM000685.1:g.43809029C= GRCh37
NC_000023.9:g.43693973C= NCBI36
NG_009832.1:g.28893G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000642620.1:c.*16G= (NDP) MANE Select ENSP00000495972.1:n.*16G=
ENST00000647044.1:c.*16G= (NDP) ENSP00000495811.1:n.*16G=
ENST00000378062.5:c.*16G= (NDP) ENSP00000367301.5:n.*16G=
ENST00000470584.1:n.462G= (NDP)
NM_000266.3:c.*16G= (NDP) NP_000257.1:n.*16G=
NR_046631.1:n.52C= (NDP-AS1)
NM_000266.4:c.*16G= (NDP) MANE Select NP_000257.1:n.*16G=