Canonical Allele Identifier: CA11398142

Gene: SLC6A6

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14439270T>C , CM000665.2:g.14439270T>C	GRCh38
NC_000003.11:g.14480778T>C , CM000665.1:g.14480778T>C	GRCh37
NC_000003.10:g.14455782T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622186.5:c.-11-4354T>C MANE Select	ENSP00000480890.1:n.-11-4354T>C
ENST00000649500.1:c.297-4354T>C	ENSP00000497250.1:n.297-4354T>C
ENST00000452775.1:c.-11-4354T>C	ENSP00000402059.1:n.-11-4354T>C
ENST00000610642.4:c.297-4354T>C	ENSP00000482391.1:n.297-4354T>C
ENST00000613060.4:c.297-4358T>C	ENSP00000481625.1:n.297-4358T>C
ENST00000613930.4:n.270-4354T>C
ENST00000615188.1:n.243-6447T>C
ENST00000618278.4:c.297-4358T>C	ENSP00000481946.1:n.297-4358T>C
ENST00000621751.4:c.-11-4354T>C	ENSP00000482560.1:n.-11-4354T>C
ENST00000622176.4:c.266-4354T>C
ENST00000622186.4:c.-11-4354T>C	ENSP00000480890.1:n.-11-4354T>C
NM_001134367.3:c.297-4358T>C	NP_001127839.2:n.297-4358T>C
NM_001134368.3:c.-11-4354T>C	NP_001127840.1:n.-11-4354T>C
NM_003043.5:c.-11-4354T>C	NP_003034.2:n.-11-4354T>C
NR_103507.2:n.315-4354T>C
XM_006713307.1:c.77-4354T>C	XP_006713370.1:n.77-4354T>C
XM_011534029.1:c.-11-4354T>C	XP_011532331.1:n.-11-4354T>C
XM_011534030.1:c.-11-4354T>C	XP_011532332.1:n.-11-4354T>C
XM_011534031.1:c.-653-4354T>C	XP_011532333.1:n.-653-4354T>C
XR_427286.1:n.119-4354T>C
XR_940495.1:n.119-4354T>C
XM_006713307.2:c.77-4354T>C	XP_006713370.1:n.77-4354T>C
XM_011534030.2:c.-11-4354T>C	XP_011532332.1:n.-11-4354T>C
XM_011534031.2:c.-653-4354T>C	XP_011532333.1:n.-653-4354T>C
XR_427286.2:n.119-4354T>C
XR_940495.3:n.119-4354T>C
NM_001134368.4:c.-11-4354T>C	NP_001127840.1:n.-11-4354T>C
NR_103507.3:n.285-4354T>C
NM_003043.6:c.-11-4354T>C MANE Select	NP_003034.2:n.-11-4354T>C