Canonical Allele Identifier: CA1361820009
Gene: SLC6A20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.45772637_45772638delinsGT , CM000665.2:g.45772637_45772638delinsGT GRCh38
NC_000003.11:g.45814129_45814130delinsGT , CM000665.1:g.45814129_45814130delinsGT GRCh37
NC_000003.10:g.45789133_45789134delinsGT NCBI36
NG_023204.1:g.28906_28907delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000703343.1:c.583-23_583-22delinsAC ENSP00000515266.1:n.583-23_583-22delinsAC
ENST00000358525.9:c.583-23_583-22delinsAC MANE Select ENSP00000346298.4:n.583-23_583-22delinsAC
ENST00000353278.8:c.583-1180_583-1179delinsAC ENSP00000296133.5:n.583-1180_583-1179delinsAC
ENST00000358525.8:c.583-23_583-22delinsAC ENSP00000346298.4:n.583-23_583-22delinsAC
ENST00000413781.1:c.442-23_442-22delinsAC ENSP00000395506.1:n.442-23_442-22delinsAC
ENST00000456124.6:c.583-23_583-22delinsAC ENSP00000404310.2:n.583-23_583-22delinsAC
NM_020208.3:c.583-23_583-22delinsAC NP_064593.1:n.583-23_583-22delinsAC
NM_022405.3:c.583-1180_583-1179delinsAC NP_071800.1:n.583-1180_583-1179delinsAC
XM_005265236.2:c.583-23_583-22delinsAC XP_005265293.1:n.583-23_583-22delinsAC
XM_011533847.1:c.286-23_286-22delinsAC XP_011532149.1:n.286-23_286-22delinsAC
XM_011533848.1:c.583-23_583-22delinsAC XP_011532150.1:n.583-23_583-22delinsAC
XM_011533847.2:c.286-23_286-22delinsAC XP_011532149.1:n.286-23_286-22delinsAC
XM_011533848.2:c.583-23_583-22delinsAC XP_011532150.1:n.583-23_583-22delinsAC
NM_020208.4:c.583-23_583-22delinsAC MANE Select NP_064593.1:n.583-23_583-22delinsAC
NM_022405.4:c.583-1180_583-1179delinsAC NP_071800.1:n.583-1180_583-1179delinsAC
NM_001385683.1:c.583-23_583-22delinsAC NP_001372612.1:n.583-23_583-22delinsAC