Canonical Allele Identifier: CA516139471

Linked Data

MyVariant Identifiers: chrX:g.43809153G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949907G>C , CM000685.2:g.43949907G>C GRCh38
NC_000023.10:g.43809153G>C , CM000685.1:g.43809153G>C GRCh37
NC_000023.9:g.43694097G>C NCBI36
NG_009832.1:g.28769C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000642620.1:c.294C>G (NDP) MANE Select ENSP00000495972.1:p.Pro98=
ENST00000647044.1:c.294C>G (NDP) ENSP00000495811.1:p.Pro98=
ENST00000378062.5:c.294C>G (NDP) ENSP00000367301.5:p.Pro98=
ENST00000470584.1:n.338C>G (NDP)
NM_000266.3:c.294C>G (NDP) NP_000257.1:p.Pro98=
NR_046631.1:n.176G>C (NDP-AS1)
NM_000266.4:c.294C>G (NDP) MANE Select NP_000257.1:p.Pro98=