Canonical Allele Identifier: CA415087450

Gene: SLC6A8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153694372A>G , CM000685.2:g.153694372A>G	GRCh38
NC_000023.10:g.152959827A>G , CM000685.1:g.152959827A>G	GRCh37
NC_000023.9:g.152613021A>G	NCBI36
NG_012016.1:g.11076A>G
NG_012016.2:g.11076A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_005629.4:c.1421A>G MANE Select	NP_005620.1:p.Asp474Gly
ENST00000253122.10:c.1421A>G MANE Select	ENSP00000253122.5:p.Asp474Gly
NM_001142805.1:c.1391A>G	NP_001136277.1:p.Asp464Gly
NM_001142805.2:c.1391A>G	NP_001136277.1:p.Asp464Gly
NM_001142806.1:c.1076A>G	NP_001136278.1:p.Asp359Gly
NM_005629.3:c.1421A>G	NP_005620.1:p.Asp474Gly
ENST00000253122.9:c.1421A>G	ENSP00000253122.5:p.Asp474Gly
ENST00000413787.1:c.350A>G	ENSP00000400463.1:p.Asp117Gly
ENST00000430077.6:c.1076A>G	ENSP00000403041.2:p.Asp359Gly
ENST00000442457.1:c.475A>G
ENST00000485324.1:n.1642A>G