Canonical Allele Identifier: CA1880239106

Gene: SLC27A4

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128345277T= , CM000671.2:g.128345277T=	GRCh38
NC_000009.11:g.131107556T= , CM000671.1:g.131107556T=	GRCh37
NC_000009.10:g.130147377T=	NCBI36
NG_017057.1:g.9718T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000300456.5:c.284T= MANE Select	ENSP00000300456.3:p.Phe95=
ENST00000300456.4:c.284T=	ENSP00000300456.3:p.Phe95=
ENST00000372870.5:c.231+1996T=	ENSP00000361961.1:n.231+1996T=
NM_005094.3:c.284T=	NP_005085.2:p.Phe95=
XM_017014222.1:c.284T=	XP_016869711.1:p.Phe95=
XM_024447391.1:c.284T=	XP_024303159.1:p.Phe95=
NM_005094.4:c.284T= MANE Select	NP_005085.2:p.Phe95=