Canonical Allele Identifier: CA1275308230
Gene: SLC9A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102532560G= , CM000664.2:g.102532560G= GRCh38
NC_000002.11:g.103149019G= , CM000664.1:g.103149019G= GRCh37
NC_000002.10:g.102515451G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000295269.5:c.2269G= MANE Select ENSP00000295269.4:p.Glu757=
ENST00000295269.4:c.2269G= ENSP00000295269.4:p.Glu757=
NM_001011552.3:c.2269G= NP_001011552.2:p.Glu757=
XM_011511158.1:c.2182G= XP_011509460.1:p.Glu728=
NM_001011552.4:c.2269G= MANE Select NP_001011552.2:p.Glu757=