Canonical Allele Identifier: CA474956136

Gene: SLC22A12

Linked Data

• MyVariant Identifiers: chr11:g.64366033G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64598561G>C , CM000673.2:g.64598561G>C	GRCh38
NC_000011.9:g.64366033G>C , CM000673.1:g.64366033G>C	GRCh37
NC_000011.8:g.64122609G>C	NCBI36
NG_008110.1:g.12752G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377574.6:c.876G>C MANE Select	ENSP00000366797.1:p.Leu292=
ENST00000336464.7:c.774G>C	ENSP00000336836.7:p.Leu258=
ENST00000377567.6:c.552G>C	ENSP00000366790.2:p.Leu184=
ENST00000377572.5:c.552G>C	ENSP00000366795.1:p.Leu184=
ENST00000377574.5:c.876G>C	ENSP00000366797.1:p.Leu292=
ENST00000473690.5:c.213G>C	ENSP00000438437.1:p.Leu71=
NM_001276326.1:c.774G>C	NP_001263255.1:p.Leu258=
NM_001276327.1:c.552G>C	NP_001263256.1:p.Leu184=
NM_144585.3:c.876G>C	NP_653186.2:p.Leu292=
NM_153378.2:c.213G>C	NP_700357.1:p.Leu71=
XM_006718430.2:c.951G>C	XP_006718493.1:p.Leu317=
XM_006718431.2:c.846G>C	XP_006718494.1:p.Leu282=
XM_006718430.4:c.951G>C	XP_006718493.1:p.Leu317=
XM_006718431.4:c.846G>C	XP_006718494.1:p.Leu282=
NM_144585.4:c.876G>C MANE Select	NP_653186.2:p.Leu292=
NM_001276326.2:c.774G>C	NP_001263255.1:p.Leu258=
NM_153378.3:c.213G>C	NP_700357.1:p.Leu71=
NM_001276327.2:c.552G>C	NP_001263256.1:p.Leu184=