Canonical Allele Identifier: CA2577572475

Gene: SLC6A20

Linked Data

• gnomAD v4: 3-45772414-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.45772414C>A , CM000665.2:g.45772414C>A	GRCh38
NC_000003.11:g.45813906C>A , CM000665.1:g.45813906C>A	GRCh37
NC_000003.10:g.45788910C>A	NCBI36
NG_023204.1:g.29130G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703343.1:c.693+91G>T	ENSP00000515266.1:n.693+91G>T
ENST00000358525.9:c.693+91G>T MANE Select	ENSP00000346298.4:n.693+91G>T
ENST00000353278.8:c.583-956G>T	ENSP00000296133.5:n.583-956G>T
ENST00000358525.8:c.693+91G>T	ENSP00000346298.4:n.693+91G>T
ENST00000413781.1:c.552+91G>T	ENSP00000395506.1:n.552+91G>T
ENST00000456124.6:c.693+91G>T	ENSP00000404310.2:n.693+91G>T
NM_020208.3:c.693+91G>T	NP_064593.1:n.693+91G>T
NM_022405.3:c.583-956G>T	NP_071800.1:n.583-956G>T
XM_005265236.2:c.693+91G>T	XP_005265293.1:n.693+91G>T
XM_011533847.1:c.396+91G>T	XP_011532149.1:n.396+91G>T
XM_011533848.1:c.693+91G>T	XP_011532150.1:n.693+91G>T
XM_011533847.2:c.396+91G>T	XP_011532149.1:n.396+91G>T
XM_011533848.2:c.693+91G>T	XP_011532150.1:n.693+91G>T
NM_020208.4:c.693+91G>T MANE Select	NP_064593.1:n.693+91G>T
NM_022405.4:c.583-956G>T	NP_071800.1:n.583-956G>T
NM_001385683.1:c.693+91G>T	NP_001372612.1:n.693+91G>T