Canonical Allele Identifier: CA474956150

Gene: SLC22A12

Linked Data

• gnomAD v4: 11-64598573-G-T
• MyVariant Identifiers: chr11:g.64366045G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64598573G>T , CM000673.2:g.64598573G>T	GRCh38
NC_000011.9:g.64366045G>T , CM000673.1:g.64366045G>T	GRCh37
NC_000011.8:g.64122621G>T	NCBI36
NG_008110.1:g.12764G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377574.6:c.888G>T MANE Select	ENSP00000366797.1:p.Leu296=
ENST00000336464.7:c.786G>T	ENSP00000336836.7:p.Leu262=
ENST00000377567.6:c.564G>T	ENSP00000366790.2:p.Leu188=
ENST00000377572.5:c.564G>T	ENSP00000366795.1:p.Leu188=
ENST00000377574.5:c.888G>T	ENSP00000366797.1:p.Leu296=
ENST00000473690.5:c.225G>T	ENSP00000438437.1:p.Leu75=
NM_001276326.1:c.786G>T	NP_001263255.1:p.Leu262=
NM_001276327.1:c.564G>T	NP_001263256.1:p.Leu188=
NM_144585.3:c.888G>T	NP_653186.2:p.Leu296=
NM_153378.2:c.225G>T	NP_700357.1:p.Leu75=
XM_006718430.2:c.963G>T	XP_006718493.1:p.Leu321=
XM_006718431.2:c.858G>T	XP_006718494.1:p.Leu286=
XM_006718430.4:c.963G>T	XP_006718493.1:p.Leu321=
XM_006718431.4:c.858G>T	XP_006718494.1:p.Leu286=
NM_144585.4:c.888G>T MANE Select	NP_653186.2:p.Leu296=
NM_001276326.2:c.786G>T	NP_001263255.1:p.Leu262=
NM_153378.3:c.225G>T	NP_700357.1:p.Leu75=
NM_001276327.2:c.564G>T	NP_001263256.1:p.Leu188=