Canonical Allele Identifier: CA375029804
Gene: SLC27A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.131107553T>C (hg19) chr9:g.128345274T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.128345274T>C , CM000671.2:g.128345274T>C GRCh38
NC_000009.11:g.131107553T>C , CM000671.1:g.131107553T>C GRCh37
NC_000009.10:g.130147374T>C NCBI36
NG_017057.1:g.9715T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000300456.5:c.281T>C MANE Select ENSP00000300456.3:p.Ile94Thr
ENST00000300456.4:c.281T>C ENSP00000300456.3:p.Ile94Thr
ENST00000372870.5:c.231+1993T>C ENSP00000361961.1:n.231+1993T>C
NM_005094.3:c.281T>C NP_005085.2:p.Ile94Thr
XM_017014222.1:c.281T>C XP_016869711.1:p.Ile94Thr
XM_024447391.1:c.281T>C XP_024303159.1:p.Ile94Thr
NM_005094.4:c.281T>C MANE Select NP_005085.2:p.Ile94Thr
Search 100 bp 5'
Search 100 bp 3'