Canonical Allele Identifier: CA2426745292

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949966C= , CM000685.2:g.43949966C= GRCh38
NC_000023.10:g.43809212C= , CM000685.1:g.43809212C= GRCh37
NC_000023.9:g.43694156C= NCBI36
NG_009832.1:g.28710G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000642620.1:c.235G= (NDP) MANE Select ENSP00000495972.1:p.Val79=
ENST00000647044.1:c.235G= (NDP) ENSP00000495811.1:p.Val79=
ENST00000378062.5:c.235G= (NDP) ENSP00000367301.5:p.Val79=
ENST00000470584.1:n.279G= (NDP)
NM_000266.3:c.235G= (NDP) NP_000257.1:p.Val79=
NR_046631.1:n.235C= (NDP-AS1)
NM_000266.4:c.235G= (NDP) MANE Select NP_000257.1:p.Val79=