Canonical Allele Identifier: CA467482909
Gene: SLC27A4 HGNC NCBI

Linked Data

dbSNP Id: rs1832634893
COSMIC: COSM5963916
MyVariant Identifiers: chr9:g.131107458G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.128345179G>A , CM000671.2:g.128345179G>A GRCh38
NC_000009.11:g.131107458G>A , CM000671.1:g.131107458G>A GRCh37
NC_000009.10:g.130147279G>A NCBI36
NG_017057.1:g.9620G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000300456.5:c.186G>A MANE Select ENSP00000300456.3:p.Val62=
ENST00000300456.4:c.186G>A ENSP00000300456.3:p.Val62=
ENST00000372870.5:c.231+1898G>A ENSP00000361961.1:n.231+1898G>A
NM_005094.3:c.186G>A NP_005085.2:p.Val62=
XM_017014222.1:c.186G>A XP_016869711.1:p.Val62=
XM_024447391.1:c.186G>A XP_024303159.1:p.Val62=
NM_005094.4:c.186G>A MANE Select NP_005085.2:p.Val62=
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