Canonical Allele Identifier: CA2426745271

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949902G= , CM000685.2:g.43949902G= GRCh38
NC_000023.10:g.43809148G= , CM000685.1:g.43809148G= GRCh37
NC_000023.9:g.43694092G= NCBI36
NG_009832.1:g.28774C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000642620.1:c.299C= (NDP) MANE Select ENSP00000495972.1:p.Thr100=
ENST00000647044.1:c.299C= (NDP) ENSP00000495811.1:p.Thr100=
ENST00000378062.5:c.299C= (NDP) ENSP00000367301.5:p.Thr100=
ENST00000470584.1:n.343C= (NDP)
NM_000266.3:c.299C= (NDP) NP_000257.1:p.Thr100=
NR_046631.1:n.171G= (NDP-AS1)
NM_000266.4:c.299C= (NDP) MANE Select NP_000257.1:p.Thr100=