Canonical Allele Identifier: CA433447618

Gene: SLC6A20

Linked Data

• MyVariant Identifiers: chr3:g.45813997C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.45772505C>T , CM000665.2:g.45772505C>T	GRCh38
NC_000003.11:g.45813997C>T , CM000665.1:g.45813997C>T	GRCh37
NC_000003.10:g.45789001C>T	NCBI36
NG_023204.1:g.29039G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703343.1:c.693G>A	ENSP00000515266.1:p.Lys231=
ENST00000358525.9:c.693G>A MANE Select	ENSP00000346298.4:p.Lys231=
ENST00000353278.8:c.583-1047G>A	ENSP00000296133.5:n.583-1047G>A
ENST00000358525.8:c.693G>A	ENSP00000346298.4:p.Lys231=
ENST00000413781.1:c.552G>A	ENSP00000395506.1:p.Lys184=
ENST00000456124.6:c.693G>A	ENSP00000404310.2:p.Lys231=
NM_020208.3:c.693G>A	NP_064593.1:p.Lys231=
NM_022405.3:c.583-1047G>A	NP_071800.1:n.583-1047G>A
XM_005265236.2:c.693G>A	XP_005265293.1:p.Lys231=
XM_011533847.1:c.396G>A	XP_011532149.1:p.Lys132=
XM_011533848.1:c.693G>A	XP_011532150.1:p.Lys231=
XM_011533847.2:c.396G>A	XP_011532149.1:p.Lys132=
XM_011533848.2:c.693G>A	XP_011532150.1:p.Lys231=
NM_020208.4:c.693G>A MANE Select	NP_064593.1:p.Lys231=
NM_022405.4:c.583-1047G>A	NP_071800.1:n.583-1047G>A
NM_001385683.1:c.693G>A	NP_001372612.1:p.Lys231=