Canonical Allele Identifier: CA2426745272

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949904C= , CM000685.2:g.43949904C= GRCh38
NC_000023.10:g.43809150C= , CM000685.1:g.43809150C= GRCh37
NC_000023.9:g.43694094C= NCBI36
NG_009832.1:g.28772G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000642620.1:c.297G= (NDP) MANE Select ENSP00000495972.1:p.Gln99=
ENST00000647044.1:c.297G= (NDP) ENSP00000495811.1:p.Gln99=
ENST00000378062.5:c.297G= (NDP) ENSP00000367301.5:p.Gln99=
ENST00000470584.1:n.341G= (NDP)
NM_000266.3:c.297G= (NDP) NP_000257.1:p.Gln99=
NR_046631.1:n.173C= (NDP-AS1)
NM_000266.4:c.297G= (NDP) MANE Select NP_000257.1:p.Gln99=