Canonical Allele Identifier: CA1676923537

Gene: SLC22A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160139693A= , CM000668.2:g.160139693A=	GRCh38
NC_000006.11:g.160560725A= , CM000668.1:g.160560725A=	GRCh37
NC_000006.10:g.160480715A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366963.9:c.1102A= MANE Select	ENSP00000355930.4:p.Met368=
ENST00000324965.8:c.1102A=	ENSP00000318103.4:p.Met368=
ENST00000366963.8:c.1102A=	ENSP00000355930.4:p.Met368=
ENST00000457470.6:c.1102A=	ENSP00000409557.2:p.Met368=
ENST00000460902.2:c.1061+3043A=	ENSP00000439274.1:n.1061+3043A=
ENST00000539263.5:c.*575A=	ENSP00000443245.1:n.*575A=
NM_003057.2:c.1102A=	NP_003048.1:p.Met368=
NM_153187.1:c.1102A=	NP_694857.1:p.Met368=
XM_005267102.3:c.1102A=	XP_005267159.1:p.Met368=
XM_005267103.1:c.1102A=	XP_005267160.1:p.Met368=
XM_005267104.3:c.526A=	XP_005267161.1:p.Met176=
XM_005267105.3:c.526A=	XP_005267162.1:p.Met176=
XM_006715552.1:c.1102A=	XP_006715615.1:p.Met368=
XM_011536074.1:c.526A=	XP_011534376.1:p.Met176=
XM_005267102.5:c.1102A=	XP_005267159.1:p.Met368=
XM_005267103.2:c.1102A=	XP_005267160.1:p.Met368=
XM_005267104.5:c.526A=	XP_005267161.1:p.Met176=
XM_005267105.5:c.526A=	XP_005267162.1:p.Met176=
XM_006715552.2:c.1102A=	XP_006715615.1:p.Met368=
XM_011536074.3:c.526A=	XP_011534376.1:p.Met176=
NM_003057.3:c.1102A= MANE Select	NP_003048.1:p.Met368=
NM_153187.2:c.1102A=	NP_694857.1:p.Met368=