Canonical Allele Identifier: CA1275308285
Gene: SLC9A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102532657G= , CM000664.2:g.102532657G= GRCh38
NC_000002.11:g.103149116G= , CM000664.1:g.103149116G= GRCh37
NC_000002.10:g.102515548G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000295269.5:c.2366G= MANE Select ENSP00000295269.4:p.Arg789=
ENST00000295269.4:c.2366G= ENSP00000295269.4:p.Arg789=
NM_001011552.3:c.2366G= NP_001011552.2:p.Arg789=
XM_011511158.1:c.2279G= XP_011509460.1:p.Arg760=
NM_001011552.4:c.2366G= MANE Select NP_001011552.2:p.Arg789=