Canonical Allele Identifier: CA1606675113

Gene: SLC22A23

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.3433084T= , CM000668.2:g.3433084T=	GRCh38
NC_000006.11:g.3433318T= , CM000668.1:g.3433318T=	GRCh37
NC_000006.10:g.3378317T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406686.8:c.655-17229A= MANE Select	ENSP00000385028.3:n.655-17229A=
ENST00000380298.2:c.655-17229A=	ENSP00000369653.2:n.655-17229A=
ENST00000380302.8:c.-190+11735A=	ENSP00000369657.4:n.-190+11735A=
ENST00000406686.7:c.655-17229A=	ENSP00000385028.3:n.655-17229A=
ENST00000436008.6:c.655-17229A=	ENSP00000410245.2:n.655-17229A=
ENST00000467177.5:c.132+5400A=	ENSP00000418985.1:n.132+5400A=
ENST00000485307.5:c.139-17229A=	ENSP00000418134.1:n.139-17229A=
ENST00000490273.5:c.-434-746A=	ENSP00000419463.1:n.-434-746A=
ENST00000497691.5:c.-190+11735A=	ENSP00000417737.1:n.-190+11735A=
NM_001286455.1:c.-190+11735A=	NP_001273384.1:n.-190+11735A=
NM_001286456.1:c.655-17229A=	NP_001273385.1:n.655-17229A=
NM_015482.1:c.655-17229A=	NP_056297.1:n.655-17229A=
NM_021945.6:c.-434-746A=	NP_068764.3:n.-434-746A=
NR_104448.1:n.195+11735A=
XM_005249285.2:c.655-17229A=	XP_005249342.1:n.655-17229A=
XM_011514801.1:c.726+5400A=	XP_011513103.1:n.726+5400A=
XM_011514801.2:c.726+5400A=	XP_011513103.1:n.726+5400A=
XM_017011180.1:c.132+5400A=	XP_016866669.1:n.132+5400A=
XM_017011183.1:c.726+5400A=	XP_016866672.1:n.726+5400A=
XM_017011185.2:c.726+5400A=	XP_016866674.1:n.726+5400A=
XM_017011186.1:c.-190+5400A=	XP_016866675.1:n.-190+5400A=
XR_001743575.1:n.726+5400A=
NM_001286456.2:c.655-17229A=	NP_001273385.1:n.655-17229A=
NM_001382317.1:c.655-17229A=	NP_001369246.1:n.655-17229A=
NM_001382320.1:c.654+22822A=	NP_001369249.1:n.654+22822A=
NM_015482.2:c.655-17229A= MANE Select	NP_056297.1:n.655-17229A=
NR_168069.1:n.1145+22822A=