Canonical Allele Identifier: CA1361819842

Gene: SLC6A20

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.45772520G= , CM000665.2:g.45772520G=	GRCh38
NC_000003.11:g.45814012G= , CM000665.1:g.45814012G=	GRCh37
NC_000003.10:g.45789016G=	NCBI36
NG_023204.1:g.29024C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703343.1:c.678C=	ENSP00000515266.1:p.Tyr226=
ENST00000358525.9:c.678C= MANE Select	ENSP00000346298.4:p.Tyr226=
ENST00000353278.8:c.583-1062C=	ENSP00000296133.5:n.583-1062C=
ENST00000358525.8:c.678C=	ENSP00000346298.4:p.Tyr226=
ENST00000413781.1:c.537C=	ENSP00000395506.1:p.Tyr179=
ENST00000456124.6:c.678C=	ENSP00000404310.2:p.Tyr226=
NM_020208.3:c.678C=	NP_064593.1:p.Tyr226=
NM_022405.3:c.583-1062C=	NP_071800.1:n.583-1062C=
XM_005265236.2:c.678C=	XP_005265293.1:p.Tyr226=
XM_011533847.1:c.381C=	XP_011532149.1:p.Tyr127=
XM_011533848.1:c.678C=	XP_011532150.1:p.Tyr226=
XM_011533847.2:c.381C=	XP_011532149.1:p.Tyr127=
XM_011533848.2:c.678C=	XP_011532150.1:p.Tyr226=
NM_020208.4:c.678C= MANE Select	NP_064593.1:p.Tyr226=
NM_022405.4:c.583-1062C=	NP_071800.1:n.583-1062C=
NM_001385683.1:c.678C=	NP_001372612.1:p.Tyr226=