Canonical Allele Identifier: CA16609140

Gene: SLC6A8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153691548C>T , CM000685.2:g.153691548C>T	GRCh38
NC_000023.10:g.152957003C>T , CM000685.1:g.152957003C>T	GRCh37
NC_000023.9:g.152610197C>T	NCBI36
NG_012016.1:g.8252C>T
NG_012016.2:g.8252C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253122.10:c.639C>T MANE Select	ENSP00000253122.5:p.Phe213=
ENST00000675713.1:n.393C>T
ENST00000253122.9:c.639C>T	ENSP00000253122.5:p.Phe213=
ENST00000429147.1:c.88C>T
ENST00000430077.6:c.294C>T	ENSP00000403041.2:p.Phe98=
ENST00000466243.1:n.431C>T
ENST00000467402.1:n.145+41C>T
NM_001142805.1:c.639C>T	NP_001136277.1:p.Phe213=
NM_001142806.1:c.294C>T	NP_001136278.1:p.Phe98=
NM_005629.3:c.639C>T	NP_005620.1:p.Phe213=
NM_005629.4:c.639C>T MANE Select	NP_005620.1:p.Phe213=
NM_001142805.2:c.639C>T	NP_001136277.1:p.Phe213=