Canonical Allele Identifier: CA413007326

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949843A>C , CM000685.2:g.43949843A>C GRCh38
NC_000023.10:g.43809089A>C , CM000685.1:g.43809089A>C GRCh37
NC_000023.9:g.43694033A>C NCBI36
NG_009832.1:g.28833T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000642620.1:c.358T>G (NDP) MANE Select ENSP00000495972.1:p.Tyr120Asp
ENST00000647044.1:c.358T>G (NDP) ENSP00000495811.1:p.Tyr120Asp
ENST00000378062.5:c.358T>G (NDP) ENSP00000367301.5:p.Tyr120Asp
ENST00000470584.1:n.402T>G (NDP)
NM_000266.3:c.358T>G (NDP) NP_000257.1:p.Tyr120Asp
NR_046631.1:n.112A>C (NDP-AS1)
NM_000266.4:c.358T>G (NDP) MANE Select NP_000257.1:p.Tyr120Asp