Canonical Allele Identifier: CA352456582

Gene: SLC6A20

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.45775926A>T , CM000665.2:g.45775926A>T	GRCh38
NC_000003.11:g.45817418A>T , CM000665.1:g.45817418A>T	GRCh37
NC_000003.10:g.45792422A>T	NCBI36
NG_023204.1:g.25618T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703343.1:c.417T>A	ENSP00000515266.1:p.Cys139Ter
ENST00000703344.1:n.489T>A
ENST00000358525.9:c.417T>A MANE Select	ENSP00000346298.4:p.Cys139Ter
ENST00000353278.8:c.417T>A	ENSP00000296133.5:p.Cys139Ter
ENST00000358525.8:c.417T>A	ENSP00000346298.4:p.Cys139Ter
ENST00000413781.1:c.276T>A	ENSP00000395506.1:p.Cys92Ter
ENST00000456124.6:c.417T>A	ENSP00000404310.2:p.Cys139Ter
NM_020208.3:c.417T>A	NP_064593.1:p.Cys139Ter
NM_022405.3:c.417T>A	NP_071800.1:p.Cys139Ter
XM_005265236.2:c.417T>A	XP_005265293.1:p.Cys139Ter
XM_011533847.1:c.120T>A	XP_011532149.1:p.Cys40Ter
XM_011533848.1:c.417T>A	XP_011532150.1:p.Cys139Ter
XM_011533847.2:c.120T>A	XP_011532149.1:p.Cys40Ter
XM_011533848.2:c.417T>A	XP_011532150.1:p.Cys139Ter
NM_020208.4:c.417T>A MANE Select	NP_064593.1:p.Cys139Ter
NM_022405.4:c.417T>A	NP_071800.1:p.Cys139Ter
NM_001385683.1:c.417T>A	NP_001372612.1:p.Cys139Ter