Canonical Allele Identifier: CA352454119

Gene: SLC6A20

Linked Data

• MyVariant Identifiers: chr3:g.45814058A>T (hg19) ; chr3:g.45772566A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.45772566A>T , CM000665.2:g.45772566A>T	GRCh38
NC_000003.11:g.45814058A>T , CM000665.1:g.45814058A>T	GRCh37
NC_000003.10:g.45789062A>T	NCBI36
NG_023204.1:g.28978T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703343.1:c.632T>A	ENSP00000515266.1:p.Leu211His
ENST00000358525.9:c.632T>A MANE Select	ENSP00000346298.4:p.Leu211His
ENST00000353278.8:c.583-1108T>A	ENSP00000296133.5:n.583-1108T>A
ENST00000358525.8:c.632T>A	ENSP00000346298.4:p.Leu211His
ENST00000413781.1:c.491T>A	ENSP00000395506.1:p.Leu164His
ENST00000456124.6:c.632T>A	ENSP00000404310.2:p.Leu211His
NM_020208.3:c.632T>A	NP_064593.1:p.Leu211His
NM_022405.3:c.583-1108T>A	NP_071800.1:n.583-1108T>A
XM_005265236.2:c.632T>A	XP_005265293.1:p.Leu211His
XM_011533847.1:c.335T>A	XP_011532149.1:p.Leu112His
XM_011533848.1:c.632T>A	XP_011532150.1:p.Leu211His
XM_011533847.2:c.335T>A	XP_011532149.1:p.Leu112His
XM_011533848.2:c.632T>A	XP_011532150.1:p.Leu211His
NM_020208.4:c.632T>A MANE Select	NP_064593.1:p.Leu211His
NM_022405.4:c.583-1108T>A	NP_071800.1:n.583-1108T>A
NM_001385683.1:c.632T>A	NP_001372612.1:p.Leu211His