Canonical Allele Identifier: CA1361819822

Gene: SLC6A20

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.45772492_45772493delinsCT , CM000665.2:g.45772492_45772493delinsCT	GRCh38
NC_000003.11:g.45813984_45813985delinsCT , CM000665.1:g.45813984_45813985delinsCT	GRCh37
NC_000003.10:g.45788988_45788989delinsCT	NCBI36
NG_023204.1:g.29051_29052delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703343.1:c.693+12_693+13delinsAG	ENSP00000515266.1:n.693+12_693+13delinsAG
ENST00000358525.9:c.693+12_693+13delinsAG MANE Select	ENSP00000346298.4:n.693+12_693+13delinsAG
ENST00000353278.8:c.583-1035_583-1034delinsAG	ENSP00000296133.5:n.583-1035_583-1034delinsAG
ENST00000358525.8:c.693+12_693+13delinsAG	ENSP00000346298.4:n.693+12_693+13delinsAG
ENST00000413781.1:c.552+12_552+13delinsAG	ENSP00000395506.1:n.552+12_552+13delinsAG
ENST00000456124.6:c.693+12_693+13delinsAG	ENSP00000404310.2:n.693+12_693+13delinsAG
NM_020208.3:c.693+12_693+13delinsAG	NP_064593.1:n.693+12_693+13delinsAG
NM_022405.3:c.583-1035_583-1034delinsAG	NP_071800.1:n.583-1035_583-1034delinsAG
XM_005265236.2:c.693+12_693+13delinsAG	XP_005265293.1:n.693+12_693+13delinsAG
XM_011533847.1:c.396+12_396+13delinsAG	XP_011532149.1:n.396+12_396+13delinsAG
XM_011533848.1:c.693+12_693+13delinsAG	XP_011532150.1:n.693+12_693+13delinsAG
XM_011533847.2:c.396+12_396+13delinsAG	XP_011532149.1:n.396+12_396+13delinsAG
XM_011533848.2:c.693+12_693+13delinsAG	XP_011532150.1:n.693+12_693+13delinsAG
NM_020208.4:c.693+12_693+13delinsAG MANE Select	NP_064593.1:n.693+12_693+13delinsAG
NM_022405.4:c.583-1035_583-1034delinsAG	NP_071800.1:n.583-1035_583-1034delinsAG
NM_001385683.1:c.693+12_693+13delinsAG	NP_001372612.1:n.693+12_693+13delinsAG