Canonical Allele Identifier: CA1275308287
Gene: SLC9A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102532659T= , CM000664.2:g.102532659T= GRCh38
NC_000002.11:g.103149118T= , CM000664.1:g.103149118T= GRCh37
NC_000002.10:g.102515550T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000295269.5:c.2368T= MANE Select ENSP00000295269.4:p.Ser790=
ENST00000295269.4:c.2368T= ENSP00000295269.4:p.Ser790=
NM_001011552.3:c.2368T= NP_001011552.2:p.Ser790=
XM_011511158.1:c.2281T= XP_011509460.1:p.Ser761=
NM_001011552.4:c.2368T= MANE Select NP_001011552.2:p.Ser790=