Canonical Allele Identifier: CA10391419

Linked Data

dbSNP Id: rs139134641
gnomAD v2: X-43809272-T-G
gnomAD v3: X-43950026-T-G
gnomAD v4: X-43950026-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43950026T>G , CM000685.2:g.43950026T>G GRCh38
NC_000023.10:g.43809272T>G , CM000685.1:g.43809272T>G GRCh37
NC_000023.9:g.43694216T>G NCBI36
NG_009832.1:g.28650A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000642620.1:c.175A>C (NDP) MANE Select ENSP00000495972.1:p.Met59Leu
ENST00000647044.1:c.175A>C (NDP) ENSP00000495811.1:p.Met59Leu
ENST00000378062.5:c.175A>C (NDP) ENSP00000367301.5:p.Met59Leu
ENST00000470584.1:n.219A>C (NDP)
NM_000266.3:c.175A>C (NDP) NP_000257.1:p.Met59Leu
NR_046631.1:n.295T>G (NDP-AS1)
NM_000266.4:c.175A>C (NDP) MANE Select NP_000257.1:p.Met59Leu