Canonical Allele Identifier: CA1880239111

Gene: SLC27A4

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128345278C= , CM000671.2:g.128345278C=	GRCh38
NC_000009.11:g.131107557C= , CM000671.1:g.131107557C=	GRCh37
NC_000009.10:g.130147378C=	NCBI36
NG_017057.1:g.9719C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000300456.5:c.285C= MANE Select	ENSP00000300456.3:p.Phe95=
ENST00000300456.4:c.285C=	ENSP00000300456.3:p.Phe95=
ENST00000372870.5:c.231+1997C=	ENSP00000361961.1:n.231+1997C=
NM_005094.3:c.285C=	NP_005085.2:p.Phe95=
XM_017014222.1:c.285C=	XP_016869711.1:p.Phe95=
XM_024447391.1:c.285C=	XP_024303159.1:p.Phe95=
NM_005094.4:c.285C= MANE Select	NP_005085.2:p.Phe95=