Canonical Allele Identifier: CA381125669

Gene: SLC22A12

Linked Data

• MyVariant Identifiers: chr11:g.64366019A>G (hg19) ; chr11:g.64598547A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64598547A>G , CM000673.2:g.64598547A>G	GRCh38
NC_000011.9:g.64366019A>G , CM000673.1:g.64366019A>G	GRCh37
NC_000011.8:g.64122595A>G	NCBI36
NG_008110.1:g.12738A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377574.6:c.862A>G MANE Select	ENSP00000366797.1:p.Thr288Ala
ENST00000336464.7:c.760A>G	ENSP00000336836.7:p.Thr254Ala
ENST00000377567.6:c.538A>G	ENSP00000366790.2:p.Thr180Ala
ENST00000377572.5:c.538A>G	ENSP00000366795.1:p.Thr180Ala
ENST00000377574.5:c.862A>G	ENSP00000366797.1:p.Thr288Ala
ENST00000473690.5:c.199A>G	ENSP00000438437.1:p.Thr67Ala
NM_001276326.1:c.760A>G	NP_001263255.1:p.Thr254Ala
NM_001276327.1:c.538A>G	NP_001263256.1:p.Thr180Ala
NM_144585.3:c.862A>G	NP_653186.2:p.Thr288Ala
NM_153378.2:c.199A>G	NP_700357.1:p.Thr67Ala
XM_006718430.2:c.937A>G	XP_006718493.1:p.Thr313Ala
XM_006718431.2:c.832A>G	XP_006718494.1:p.Thr278Ala
XM_006718430.4:c.937A>G	XP_006718493.1:p.Thr313Ala
XM_006718431.4:c.832A>G	XP_006718494.1:p.Thr278Ala
NM_144585.4:c.862A>G MANE Select	NP_653186.2:p.Thr288Ala
NM_001276326.2:c.760A>G	NP_001263255.1:p.Thr254Ala
NM_153378.3:c.199A>G	NP_700357.1:p.Thr67Ala
NM_001276327.2:c.538A>G	NP_001263256.1:p.Thr180Ala