Canonical Allele Identifier: CA1275308227
Gene: SLC9A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102532554G= , CM000664.2:g.102532554G= GRCh38
NC_000002.11:g.103149013G= , CM000664.1:g.103149013G= GRCh37
NC_000002.10:g.102515445G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000295269.5:c.2263G= MANE Select ENSP00000295269.4:p.Asp755=
ENST00000295269.4:c.2263G= ENSP00000295269.4:p.Asp755=
NM_001011552.3:c.2263G= NP_001011552.2:p.Asp755=
XM_011511158.1:c.2176G= XP_011509460.1:p.Asp726=
NM_001011552.4:c.2263G= MANE Select NP_001011552.2:p.Asp755=