Canonical Allele Identifier: CA474956069

Gene: SLC22A12

Linked Data

• MyVariant Identifiers: chr11:g.64366006A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64598534A>T , CM000673.2:g.64598534A>T	GRCh38
NC_000011.9:g.64366006A>T , CM000673.1:g.64366006A>T	GRCh37
NC_000011.8:g.64122582A>T	NCBI36
NG_008110.1:g.12725A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377574.6:c.849A>T MANE Select	ENSP00000366797.1:p.Ala283=
ENST00000336464.7:c.747A>T	ENSP00000336836.7:p.Ala249=
ENST00000377567.6:c.525A>T	ENSP00000366790.2:p.Ala175=
ENST00000377572.5:c.525A>T	ENSP00000366795.1:p.Ala175=
ENST00000377574.5:c.849A>T	ENSP00000366797.1:p.Ala283=
ENST00000473690.5:c.186A>T	ENSP00000438437.1:p.Ala62=
NM_001276326.1:c.747A>T	NP_001263255.1:p.Ala249=
NM_001276327.1:c.525A>T	NP_001263256.1:p.Ala175=
NM_144585.3:c.849A>T	NP_653186.2:p.Ala283=
NM_153378.2:c.186A>T	NP_700357.1:p.Ala62=
XM_006718430.2:c.924A>T	XP_006718493.1:p.Ala308=
XM_006718431.2:c.819A>T	XP_006718494.1:p.Ala273=
XM_006718430.4:c.924A>T	XP_006718493.1:p.Ala308=
XM_006718431.4:c.819A>T	XP_006718494.1:p.Ala273=
NM_144585.4:c.849A>T MANE Select	NP_653186.2:p.Ala283=
NM_001276326.2:c.747A>T	NP_001263255.1:p.Ala249=
NM_153378.3:c.186A>T	NP_700357.1:p.Ala62=
NM_001276327.2:c.525A>T	NP_001263256.1:p.Ala175=