Canonical Allele Identifier: CA1361819986

Gene: SLC6A20

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.45772620G= , CM000665.2:g.45772620G=	GRCh38
NC_000003.11:g.45814112G= , CM000665.1:g.45814112G=	GRCh37
NC_000003.10:g.45789116G=	NCBI36
NG_023204.1:g.28924C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703343.1:c.583-5C=	ENSP00000515266.1:n.583-5C=
ENST00000358525.9:c.583-5C= MANE Select	ENSP00000346298.4:n.583-5C=
ENST00000353278.8:c.583-1162C=	ENSP00000296133.5:n.583-1162C=
ENST00000358525.8:c.583-5C=	ENSP00000346298.4:n.583-5C=
ENST00000413781.1:c.442-5C=	ENSP00000395506.1:n.442-5C=
ENST00000456124.6:c.583-5C=	ENSP00000404310.2:n.583-5C=
NM_020208.3:c.583-5C=	NP_064593.1:n.583-5C=
NM_022405.3:c.583-1162C=	NP_071800.1:n.583-1162C=
XM_005265236.2:c.583-5C=	XP_005265293.1:n.583-5C=
XM_011533847.1:c.286-5C=	XP_011532149.1:n.286-5C=
XM_011533848.1:c.583-5C=	XP_011532150.1:n.583-5C=
XM_011533847.2:c.286-5C=	XP_011532149.1:n.286-5C=
XM_011533848.2:c.583-5C=	XP_011532150.1:n.583-5C=
NM_020208.4:c.583-5C= MANE Select	NP_064593.1:n.583-5C=
NM_022405.4:c.583-1162C=	NP_071800.1:n.583-1162C=
NM_001385683.1:c.583-5C=	NP_001372612.1:n.583-5C=