Canonical Allele Identifier: CA381125356

Gene: SLC22A12

Linked Data

• MyVariant Identifiers: chr11:g.64365987G>C (hg19) ; chr11:g.64598515G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64598515G>C , CM000673.2:g.64598515G>C	GRCh38
NC_000011.9:g.64365987G>C , CM000673.1:g.64365987G>C	GRCh37
NC_000011.8:g.64122563G>C	NCBI36
NG_008110.1:g.12706G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377574.6:c.831-1G>C MANE Select	ENSP00000366797.1:n.831-1G>C
ENST00000336464.7:c.729-1G>C	ENSP00000336836.7:n.729-1G>C
ENST00000377567.6:c.507-1G>C	ENSP00000366790.2:n.507-1G>C
ENST00000377572.5:c.507-1G>C	ENSP00000366795.1:n.507-1G>C
ENST00000377574.5:c.831-1G>C	ENSP00000366797.1:n.831-1G>C
ENST00000473690.5:c.168-1G>C	ENSP00000438437.1:n.168-1G>C
NM_001276326.1:c.729-1G>C	NP_001263255.1:n.729-1G>C
NM_001276327.1:c.507-1G>C	NP_001263256.1:n.507-1G>C
NM_144585.3:c.831-1G>C	NP_653186.2:n.831-1G>C
NM_153378.2:c.168-1G>C	NP_700357.1:n.168-1G>C
XM_006718430.2:c.906-1G>C	XP_006718493.1:n.906-1G>C
XM_006718431.2:c.801-1G>C	XP_006718494.1:n.801-1G>C
XM_006718430.4:c.906-1G>C	XP_006718493.1:n.906-1G>C
XM_006718431.4:c.801-1G>C	XP_006718494.1:n.801-1G>C
NM_144585.4:c.831-1G>C MANE Select	NP_653186.2:n.831-1G>C
NM_001276326.2:c.729-1G>C	NP_001263255.1:n.729-1G>C
NM_153378.3:c.168-1G>C	NP_700357.1:n.168-1G>C
NM_001276327.2:c.507-1G>C	NP_001263256.1:n.507-1G>C