Canonical Allele Identifier: CA352453824

Gene: SLC6A20

Linked Data

• MyVariant Identifiers: chr3:g.45814008A>C (hg19) ; chr3:g.45772516A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.45772516A>C , CM000665.2:g.45772516A>C	GRCh38
NC_000003.11:g.45814008A>C , CM000665.1:g.45814008A>C	GRCh37
NC_000003.10:g.45789012A>C	NCBI36
NG_023204.1:g.29028T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703343.1:c.682T>G	ENSP00000515266.1:p.Phe228Val
ENST00000358525.9:c.682T>G MANE Select	ENSP00000346298.4:p.Phe228Val
ENST00000353278.8:c.583-1058T>G	ENSP00000296133.5:n.583-1058T>G
ENST00000358525.8:c.682T>G	ENSP00000346298.4:p.Phe228Val
ENST00000413781.1:c.541T>G	ENSP00000395506.1:p.Phe181Val
ENST00000456124.6:c.682T>G	ENSP00000404310.2:p.Phe228Val
NM_020208.3:c.682T>G	NP_064593.1:p.Phe228Val
NM_022405.3:c.583-1058T>G	NP_071800.1:n.583-1058T>G
XM_005265236.2:c.682T>G	XP_005265293.1:p.Phe228Val
XM_011533847.1:c.385T>G	XP_011532149.1:p.Phe129Val
XM_011533848.1:c.682T>G	XP_011532150.1:p.Phe228Val
XM_011533847.2:c.385T>G	XP_011532149.1:p.Phe129Val
XM_011533848.2:c.682T>G	XP_011532150.1:p.Phe228Val
NM_020208.4:c.682T>G MANE Select	NP_064593.1:p.Phe228Val
NM_022405.4:c.583-1058T>G	NP_071800.1:n.583-1058T>G
NM_001385683.1:c.682T>G	NP_001372612.1:p.Phe228Val