Canonical Allele Identifier: CA1361819926

Gene: SLC6A20

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.45772597A= , CM000665.2:g.45772597A=	GRCh38
NC_000003.11:g.45814089A= , CM000665.1:g.45814089A=	GRCh37
NC_000003.10:g.45789093A=	NCBI36
NG_023204.1:g.28947T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703343.1:c.601T=	ENSP00000515266.1:p.Ser201=
ENST00000358525.9:c.601T= MANE Select	ENSP00000346298.4:p.Ser201=
ENST00000353278.8:c.583-1139T=	ENSP00000296133.5:n.583-1139T=
ENST00000358525.8:c.601T=	ENSP00000346298.4:p.Ser201=
ENST00000413781.1:c.460T=	ENSP00000395506.1:p.Ser154=
ENST00000456124.6:c.601T=	ENSP00000404310.2:p.Ser201=
NM_020208.3:c.601T=	NP_064593.1:p.Ser201=
NM_022405.3:c.583-1139T=	NP_071800.1:n.583-1139T=
XM_005265236.2:c.601T=	XP_005265293.1:p.Ser201=
XM_011533847.1:c.304T=	XP_011532149.1:p.Ser102=
XM_011533848.1:c.601T=	XP_011532150.1:p.Ser201=
XM_011533847.2:c.304T=	XP_011532149.1:p.Ser102=
XM_011533848.2:c.601T=	XP_011532150.1:p.Ser201=
NM_020208.4:c.601T= MANE Select	NP_064593.1:p.Ser201=
NM_022405.4:c.583-1139T=	NP_071800.1:n.583-1139T=
NM_001385683.1:c.601T=	NP_001372612.1:p.Ser201=