Canonical Allele Identifier: CA1880238918

Gene: SLC27A4

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128345178T= , CM000671.2:g.128345178T=	GRCh38
NC_000009.11:g.131107457T= , CM000671.1:g.131107457T=	GRCh37
NC_000009.10:g.130147278T=	NCBI36
NG_017057.1:g.9619T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000300456.5:c.185T= MANE Select	ENSP00000300456.3:p.Val62=
ENST00000300456.4:c.185T=	ENSP00000300456.3:p.Val62=
ENST00000372870.5:c.231+1897T=	ENSP00000361961.1:n.231+1897T=
NM_005094.3:c.185T=	NP_005085.2:p.Val62=
XM_017014222.1:c.185T=	XP_016869711.1:p.Val62=
XM_024447391.1:c.185T=	XP_024303159.1:p.Val62=
NM_005094.4:c.185T= MANE Select	NP_005085.2:p.Val62=