Canonical Allele Identifier: CA467483026
Gene: SLC27A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.131107551G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.128345272G>C , CM000671.2:g.128345272G>C GRCh38
NC_000009.11:g.131107551G>C , CM000671.1:g.131107551G>C GRCh37
NC_000009.10:g.130147372G>C NCBI36
NG_017057.1:g.9713G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000300456.5:c.279G>C MANE Select ENSP00000300456.3:p.Leu93=
ENST00000300456.4:c.279G>C ENSP00000300456.3:p.Leu93=
ENST00000372870.5:c.231+1991G>C ENSP00000361961.1:n.231+1991G>C
NM_005094.3:c.279G>C NP_005085.2:p.Leu93=
XM_017014222.1:c.279G>C XP_016869711.1:p.Leu93=
XM_024447391.1:c.279G>C XP_024303159.1:p.Leu93=
NM_005094.4:c.279G>C MANE Select NP_005085.2:p.Leu93=
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