Canonical Allele Identifier: CA417558180

Gene: SLC6A9

Linked Data

• MyVariant Identifiers: chr1:g.44467170A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.44001498A>T , CM000663.2:g.44001498A>T	GRCh38
NC_000001.10:g.44467170A>T , CM000663.1:g.44467170A>T	GRCh37
NC_000001.9:g.44239757A>T	NCBI36
NG_050929.1:g.34995T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000372310.8:c.1092T>A MANE Select	ENSP00000361384.4:p.Pro364=
ENST00000673836.1:c.1092T>A	ENSP00000501314.1:p.Pro364=
ENST00000357730.6:c.1149T>A	ENSP00000350362.2:p.Pro383=
ENST00000360584.6:c.1311T>A	ENSP00000353791.2:p.Pro437=
ENST00000372306.7:c.1092T>A	ENSP00000361380.3:p.Pro364=
ENST00000372307.7:c.897T>A	ENSP00000361381.3:p.Pro299=
ENST00000372310.7:c.1092T>A	ENSP00000361384.3:p.Pro364=
ENST00000475075.6:c.759T>A	ENSP00000434460.1:p.Pro253=
NM_001024845.2:c.1092T>A	NP_001020016.1:p.Pro364=
NM_001261380.1:c.1104T>A	NP_001248309.1:p.Pro368=
NM_006934.3:c.1149T>A	NP_008865.2:p.Pro383=
NM_201649.3:c.1311T>A	NP_964012.2:p.Pro437=
NR_048548.1:n.1356T>A
NR_048549.1:n.1075T>A
XM_011542017.1:c.1311T>A	XP_011540319.1:p.Pro437=
NM_001328626.1:c.759T>A	NP_001315555.1:p.Pro253=
NM_001328627.1:c.1029T>A	NP_001315556.1:p.Pro343=
NM_001328628.1:c.897T>A	NP_001315557.1:p.Pro299=
NM_001328629.1:c.1092T>A	NP_001315558.1:p.Pro364=
NM_001328630.1:c.759T>A	NP_001315559.1:p.Pro253=
XM_011542017.2:c.1311T>A	XP_011540319.1:p.Pro437=
XM_017002152.2:c.1011T>A	XP_016857641.1:p.Pro337=
XM_017002153.2:c.978T>A	XP_016857642.1:p.Pro326=
XM_024449295.1:c.897T>A	XP_024305063.1:p.Pro299=
NM_001024845.3:c.1092T>A MANE Select	NP_001020016.1:p.Pro364=
NM_001261380.2:c.1104T>A	NP_001248309.1:p.Pro368=
NM_001328626.2:c.759T>A	NP_001315555.1:p.Pro253=
NM_001328630.2:c.759T>A	NP_001315559.1:p.Pro253=
NM_006934.4:c.1149T>A	NP_008865.2:p.Pro383=
NM_201649.4:c.1311T>A	NP_964012.2:p.Pro437=
NR_048548.2:n.1179T>A