Canonical Allele Identifier: CA375029812
Gene: SLC27A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.131107556T>A (hg19) chr9:g.128345277T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.128345277T>A , CM000671.2:g.128345277T>A GRCh38
NC_000009.11:g.131107556T>A , CM000671.1:g.131107556T>A GRCh37
NC_000009.10:g.130147377T>A NCBI36
NG_017057.1:g.9718T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000300456.5:c.284T>A MANE Select ENSP00000300456.3:p.Phe95Tyr
ENST00000300456.4:c.284T>A ENSP00000300456.3:p.Phe95Tyr
ENST00000372870.5:c.231+1996T>A ENSP00000361961.1:n.231+1996T>A
NM_005094.3:c.284T>A NP_005085.2:p.Phe95Tyr
XM_017014222.1:c.284T>A XP_016869711.1:p.Phe95Tyr
XM_024447391.1:c.284T>A XP_024303159.1:p.Phe95Tyr
NM_005094.4:c.284T>A MANE Select NP_005085.2:p.Phe95Tyr
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