Canonical Allele Identifier: CA1275308241
Gene: SLC9A4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102532582G= , CM000664.2:g.102532582G= GRCh38
NC_000002.11:g.103149041G= , CM000664.1:g.103149041G= GRCh37
NC_000002.10:g.102515473G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000295269.5:c.2291G= MANE Select ENSP00000295269.4:p.Ser764=
ENST00000295269.4:c.2291G= ENSP00000295269.4:p.Ser764=
NM_001011552.3:c.2291G= NP_001011552.2:p.Ser764=
XM_011511158.1:c.2204G= XP_011509460.1:p.Ser735=
NM_001011552.4:c.2291G= MANE Select NP_001011552.2:p.Ser764=
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