Canonical Allele Identifier: CA1880239098

Gene: SLC27A4

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128345267G= , CM000671.2:g.128345267G=	GRCh38
NC_000009.11:g.131107546G= , CM000671.1:g.131107546G=	GRCh37
NC_000009.10:g.130147367G=	NCBI36
NG_017057.1:g.9708G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000300456.5:c.274G= MANE Select	ENSP00000300456.3:p.Ala92=
ENST00000300456.4:c.274G=	ENSP00000300456.3:p.Ala92=
ENST00000372870.5:c.231+1986G=	ENSP00000361961.1:n.231+1986G=
NM_005094.3:c.274G=	NP_005085.2:p.Ala92=
XM_017014222.1:c.274G=	XP_016869711.1:p.Ala92=
XM_024447391.1:c.274G=	XP_024303159.1:p.Ala92=
NM_005094.4:c.274G= MANE Select	NP_005085.2:p.Ala92=