Canonical Allele Identifier: CA375029282
Gene: SLC27A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.131107448T>G (hg19) chr9:g.128345169T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.128345169T>G , CM000671.2:g.128345169T>G GRCh38
NC_000009.11:g.131107448T>G , CM000671.1:g.131107448T>G GRCh37
NC_000009.10:g.130147269T>G NCBI36
NG_017057.1:g.9610T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000300456.5:c.176T>G MANE Select ENSP00000300456.3:p.Leu59Arg
ENST00000300456.4:c.176T>G ENSP00000300456.3:p.Leu59Arg
ENST00000372870.5:c.231+1888T>G ENSP00000361961.1:n.231+1888T>G
NM_005094.3:c.176T>G NP_005085.2:p.Leu59Arg
XM_017014222.1:c.176T>G XP_016869711.1:p.Leu59Arg
XM_024447391.1:c.176T>G XP_024303159.1:p.Leu59Arg
NM_005094.4:c.176T>G MANE Select NP_005085.2:p.Leu59Arg
Search 100 bp 5'
Search 100 bp 3'