Canonical Allele Identifier: CA347952137
Gene: SLC9A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102532615C>G , CM000664.2:g.102532615C>G GRCh38
NC_000002.11:g.103149074C>G , CM000664.1:g.103149074C>G GRCh37
NC_000002.10:g.102515506C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000295269.5:c.2324C>G MANE Select ENSP00000295269.4:p.Ser775Trp
ENST00000295269.4:c.2324C>G ENSP00000295269.4:p.Ser775Trp
NM_001011552.3:c.2324C>G NP_001011552.2:p.Ser775Trp
XM_011511158.1:c.2237C>G XP_011509460.1:p.Ser746Trp
NM_001011552.4:c.2324C>G MANE Select NP_001011552.2:p.Ser775Trp