Canonical Allele Identifier: CA413007244

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949807T>C , CM000685.2:g.43949807T>C GRCh38
NC_000023.10:g.43809053T>C , CM000685.1:g.43809053T>C GRCh37
NC_000023.9:g.43693997T>C NCBI36
NG_009832.1:g.28869A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000642620.1:c.394A>G (NDP) MANE Select ENSP00000495972.1:p.Asn132Asp
ENST00000647044.1:c.394A>G (NDP) ENSP00000495811.1:p.Asn132Asp
ENST00000378062.5:c.394A>G (NDP) ENSP00000367301.5:p.Asn132Asp
ENST00000470584.1:n.438A>G (NDP)
NM_000266.3:c.394A>G (NDP) NP_000257.1:p.Asn132Asp
NR_046631.1:n.76T>C (NDP-AS1)
NM_000266.4:c.394A>G (NDP) MANE Select NP_000257.1:p.Asn132Asp