Canonical Allele Identifier: CA2614173608

Gene: SLC22A12

Linked Data

• gnomAD v4: 11-64598484-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64598484C>T , CM000673.2:g.64598484C>T	GRCh38
NC_000011.9:g.64365956C>T , CM000673.1:g.64365956C>T	GRCh37
NC_000011.8:g.64122532C>T	NCBI36
NG_008110.1:g.12675C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000377574.6:c.831-32C>T MANE Select	ENSP00000366797.1:n.831-32C>T
ENST00000336464.7:c.729-32C>T	ENSP00000336836.7:n.729-32C>T
ENST00000377567.6:c.507-32C>T	ENSP00000366790.2:n.507-32C>T
ENST00000377572.5:c.507-32C>T	ENSP00000366795.1:n.507-32C>T
ENST00000377574.5:c.831-32C>T	ENSP00000366797.1:n.831-32C>T
ENST00000473690.5:c.168-32C>T	ENSP00000438437.1:n.168-32C>T
NM_001276326.1:c.729-32C>T	NP_001263255.1:n.729-32C>T
NM_001276327.1:c.507-32C>T	NP_001263256.1:n.507-32C>T
NM_144585.3:c.831-32C>T	NP_653186.2:n.831-32C>T
NM_153378.2:c.168-32C>T	NP_700357.1:n.168-32C>T
XM_006718430.2:c.906-32C>T	XP_006718493.1:n.906-32C>T
XM_006718431.2:c.801-32C>T	XP_006718494.1:n.801-32C>T
XM_006718430.4:c.906-32C>T	XP_006718493.1:n.906-32C>T
XM_006718431.4:c.801-32C>T	XP_006718494.1:n.801-32C>T
NM_144585.4:c.831-32C>T MANE Select	NP_653186.2:n.831-32C>T
NM_001276326.2:c.729-32C>T	NP_001263255.1:n.729-32C>T
NM_153378.3:c.168-32C>T	NP_700357.1:n.168-32C>T
NM_001276327.2:c.507-32C>T	NP_001263256.1:n.507-32C>T