Canonical Allele Identifier: CA453013252

Gene: SLC22A1

Linked Data

• MyVariant Identifiers: chr6:g.160575842G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160154810G>T , CM000668.2:g.160154810G>T	GRCh38
NC_000006.11:g.160575842G>T , CM000668.1:g.160575842G>T	GRCh37
NC_000006.10:g.160495832G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000366963.9:c.1398G>T MANE Select	ENSP00000355930.4:p.Val466=
ENST00000324965.8:c.1386-1165G>T	ENSP00000318103.4:n.1386-1165G>T
ENST00000366963.8:c.1398G>T	ENSP00000355930.4:p.Val466=
ENST00000457470.6:c.1386-3706G>T	ENSP00000409557.2:n.1386-3706G>T
ENST00000460902.2:c.1183G>T	ENSP00000439274.1:n.1183G>T
ENST00000539263.5:c.*871G>T	ENSP00000443245.1:n.*871G>T
NM_003057.2:c.1398G>T	NP_003048.1:p.Val466=
NM_153187.1:c.1386-1165G>T	NP_694857.1:n.1386-1165G>T
XM_005267102.3:c.1398G>T	XP_005267159.1:p.Val466=
XM_005267103.1:c.1398G>T	XP_005267160.1:p.Val466=
XM_005267104.3:c.822G>T	XP_005267161.1:p.Val274=
XM_005267105.3:c.822G>T	XP_005267162.1:p.Val274=
XM_006715552.1:c.1386-3706G>T	XP_006715615.1:n.1386-3706G>T
XM_011536074.1:c.822G>T	XP_011534376.1:p.Val274=
XM_005267102.5:c.1398G>T	XP_005267159.1:p.Val466=
XM_005267103.2:c.1398G>T	XP_005267160.1:p.Val466=
XM_005267104.5:c.822G>T	XP_005267161.1:p.Val274=
XM_005267105.5:c.822G>T	XP_005267162.1:p.Val274=
XM_006715552.2:c.1386-3706G>T	XP_006715615.1:n.1386-3706G>T
XM_011536074.3:c.822G>T	XP_011534376.1:p.Val274=
NM_003057.3:c.1398G>T MANE Select	NP_003048.1:p.Val466=
NM_153187.2:c.1386-1165G>T	NP_694857.1:n.1386-1165G>T