Canonical Allele Identifier: CA5260867
Gene: SLC27A4 HGNC NCBI

Linked Data

dbSNP Id: rs757885764
ExAC: 9:131107453 A / C
gnomAD v2: 9-131107453-A-C
gnomAD v4: 9-128345174-A-C
MyVariant Identifiers: chr9:g.131107453A>C (hg19) chr9:g.128345174A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.128345174A>C , CM000671.2:g.128345174A>C GRCh38
NC_000009.11:g.131107453A>C , CM000671.1:g.131107453A>C GRCh37
NC_000009.10:g.130147274A>C NCBI36
NG_017057.1:g.9615A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000300456.5:c.181A>C MANE Select ENSP00000300456.3:p.Lys61Gln
ENST00000300456.4:c.181A>C ENSP00000300456.3:p.Lys61Gln
ENST00000372870.5:c.231+1893A>C ENSP00000361961.1:n.231+1893A>C
NM_005094.3:c.181A>C NP_005085.2:p.Lys61Gln
XM_017014222.1:c.181A>C XP_016869711.1:p.Lys61Gln
XM_024447391.1:c.181A>C XP_024303159.1:p.Lys61Gln
NM_005094.4:c.181A>C MANE Select NP_005085.2:p.Lys61Gln
Search 100 bp 5'
Search 100 bp 3'