Canonical Allele Identifier: CA375029463
Gene: SLC27A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.128345204C>A , CM000671.2:g.128345204C>A GRCh38
NC_000009.11:g.131107483C>A , CM000671.1:g.131107483C>A GRCh37
NC_000009.10:g.130147304C>A NCBI36
NG_017057.1:g.9645C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000300456.5:c.211C>A MANE Select ENSP00000300456.3:p.Gln71Lys
ENST00000300456.4:c.211C>A ENSP00000300456.3:p.Gln71Lys
ENST00000372870.5:c.231+1923C>A ENSP00000361961.1:n.231+1923C>A
NM_005094.3:c.211C>A NP_005085.2:p.Gln71Lys
XM_017014222.1:c.211C>A XP_016869711.1:p.Gln71Lys
XM_024447391.1:c.211C>A XP_024303159.1:p.Gln71Lys
NM_005094.4:c.211C>A MANE Select NP_005085.2:p.Gln71Lys