Canonical Allele Identifier: CA453013246

Gene: SLC22A1

Linked Data

• MyVariant Identifiers: chr6:g.160575839A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160154807A>C , CM000668.2:g.160154807A>C	GRCh38
NC_000006.11:g.160575839A>C , CM000668.1:g.160575839A>C	GRCh37
NC_000006.10:g.160495829A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000366963.9:c.1395A>C MANE Select	ENSP00000355930.4:p.Gly465=
ENST00000324965.8:c.1386-1168A>C	ENSP00000318103.4:n.1386-1168A>C
ENST00000366963.8:c.1395A>C	ENSP00000355930.4:p.Gly465=
ENST00000457470.6:c.1386-3709A>C	ENSP00000409557.2:n.1386-3709A>C
ENST00000460902.2:c.1180A>C	ENSP00000439274.1:n.1180A>C
ENST00000539263.5:c.*868A>C	ENSP00000443245.1:n.*868A>C
NM_003057.2:c.1395A>C	NP_003048.1:p.Gly465=
NM_153187.1:c.1386-1168A>C	NP_694857.1:n.1386-1168A>C
XM_005267102.3:c.1395A>C	XP_005267159.1:p.Gly465=
XM_005267103.1:c.1395A>C	XP_005267160.1:p.Gly465=
XM_005267104.3:c.819A>C	XP_005267161.1:p.Gly273=
XM_005267105.3:c.819A>C	XP_005267162.1:p.Gly273=
XM_006715552.1:c.1386-3709A>C	XP_006715615.1:n.1386-3709A>C
XM_011536074.1:c.819A>C	XP_011534376.1:p.Gly273=
XM_005267102.5:c.1395A>C	XP_005267159.1:p.Gly465=
XM_005267103.2:c.1395A>C	XP_005267160.1:p.Gly465=
XM_005267104.5:c.819A>C	XP_005267161.1:p.Gly273=
XM_005267105.5:c.819A>C	XP_005267162.1:p.Gly273=
XM_006715552.2:c.1386-3709A>C	XP_006715615.1:n.1386-3709A>C
XM_011536074.3:c.819A>C	XP_011534376.1:p.Gly273=
NM_003057.3:c.1395A>C MANE Select	NP_003048.1:p.Gly465=
NM_153187.2:c.1386-1168A>C	NP_694857.1:n.1386-1168A>C