Canonical Allele Identifier: CA375029767
Gene: SLC27A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.131107546G>T (hg19) chr9:g.128345267G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.128345267G>T , CM000671.2:g.128345267G>T GRCh38
NC_000009.11:g.131107546G>T , CM000671.1:g.131107546G>T GRCh37
NC_000009.10:g.130147367G>T NCBI36
NG_017057.1:g.9708G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000300456.5:c.274G>T MANE Select ENSP00000300456.3:p.Ala92Ser
ENST00000300456.4:c.274G>T ENSP00000300456.3:p.Ala92Ser
ENST00000372870.5:c.231+1986G>T ENSP00000361961.1:n.231+1986G>T
NM_005094.3:c.274G>T NP_005085.2:p.Ala92Ser
XM_017014222.1:c.274G>T XP_016869711.1:p.Ala92Ser
XM_024447391.1:c.274G>T XP_024303159.1:p.Ala92Ser
NM_005094.4:c.274G>T MANE Select NP_005085.2:p.Ala92Ser
Search 100 bp 5'
Search 100 bp 3'