Canonical Allele Identifier: CA14656864

Gene: SLC27A1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17479472G>T , CM000681.2:g.17479472G>T	GRCh38
NC_000019.9:g.17590281G>T , CM000681.1:g.17590281G>T	GRCh37
NC_000019.8:g.17451281G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252595.12:c.168-7091G>T MANE Select	ENSP00000252595.6:n.168-7091G>T
ENST00000252595.11:c.168-7091G>T	ENSP00000252595.6:n.168-7091G>T
ENST00000598424.5:c.-684-4410G>T	ENSP00000472313.1:n.-684-4410G>T
ENST00000599380.5:c.168-7988G>T	ENSP00000469459.1:n.168-7988G>T
ENST00000600277.5:c.168-7091G>T	ENSP00000472082.1:n.168-7091G>T
ENST00000600297.1:c.168-7091G>T	ENSP00000469881.1:n.168-7091G>T
NM_198580.2:c.168-7091G>T	NP_940982.1:n.168-7091G>T
XM_011528000.1:c.168-7091G>T	XP_011526302.1:n.168-7091G>T
XM_011528001.1:c.168-7091G>T	XP_011526303.1:n.168-7091G>T
XM_011528002.1:c.168-7091G>T	XP_011526304.1:n.168-7091G>T
XM_011528003.1:c.168-7091G>T	XP_011526305.1:n.168-7091G>T
XR_936176.1:n.406-7091G>T
XR_936177.1:n.406-7091G>T
XM_011528001.2:c.168-7091G>T	XP_011526303.1:n.168-7091G>T
XM_011528002.2:c.168-7091G>T	XP_011526304.1:n.168-7091G>T
XM_011528003.2:c.168-7091G>T	XP_011526305.1:n.168-7091G>T
XM_017026781.1:c.168-7091G>T	XP_016882270.1:n.168-7091G>T
XR_001753680.1:n.205-7091G>T
XR_001753681.1:n.205-7091G>T
NM_198580.3:c.168-7091G>T MANE Select	NP_940982.1:n.168-7091G>T