Canonical Allele Identifier: CA1676923568

Gene: SLC22A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160139753C= , CM000668.2:g.160139753C=	GRCh38
NC_000006.11:g.160560785C= , CM000668.1:g.160560785C=	GRCh37
NC_000006.10:g.160480775C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366963.9:c.1162C= MANE Select	ENSP00000355930.4:p.Pro388=
ENST00000324965.8:c.1162C=	ENSP00000318103.4:p.Pro388=
ENST00000366963.8:c.1162C=	ENSP00000355930.4:p.Pro388=
ENST00000457470.6:c.1162C=	ENSP00000409557.2:p.Pro388=
ENST00000460902.2:c.1061+3103C=	ENSP00000439274.1:n.1061+3103C=
ENST00000539263.5:c.*635C=	ENSP00000443245.1:n.*635C=
NM_003057.2:c.1162C=	NP_003048.1:p.Pro388=
NM_153187.1:c.1162C=	NP_694857.1:p.Pro388=
XM_005267102.3:c.1162C=	XP_005267159.1:p.Pro388=
XM_005267103.1:c.1162C=	XP_005267160.1:p.Pro388=
XM_005267104.3:c.586C=	XP_005267161.1:p.Pro196=
XM_005267105.3:c.586C=	XP_005267162.1:p.Pro196=
XM_006715552.1:c.1162C=	XP_006715615.1:p.Pro388=
XM_011536074.1:c.586C=	XP_011534376.1:p.Pro196=
XM_005267102.5:c.1162C=	XP_005267159.1:p.Pro388=
XM_005267103.2:c.1162C=	XP_005267160.1:p.Pro388=
XM_005267104.5:c.586C=	XP_005267161.1:p.Pro196=
XM_005267105.5:c.586C=	XP_005267162.1:p.Pro196=
XM_006715552.2:c.1162C=	XP_006715615.1:p.Pro388=
XM_011536074.3:c.586C=	XP_011534376.1:p.Pro196=
NM_003057.3:c.1162C= MANE Select	NP_003048.1:p.Pro388=
NM_153187.2:c.1162C=	NP_694857.1:p.Pro388=