Canonical Allele Identifier: CA366330672

Gene: SLC22A1

Linked Data

• dbSNP Id: rs1781597480
• MyVariant Identifiers: chr6:g.160575847T>C (hg19) ; chr6:g.160154815T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160154815T>C , CM000668.2:g.160154815T>C	GRCh38
NC_000006.11:g.160575847T>C , CM000668.1:g.160575847T>C	GRCh37
NC_000006.10:g.160495837T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000366963.9:c.1403T>C MANE Select	ENSP00000355930.4:p.Val468Ala
ENST00000324965.8:c.1386-1160T>C	ENSP00000318103.4:n.1386-1160T>C
ENST00000366963.8:c.1403T>C	ENSP00000355930.4:p.Val468Ala
ENST00000457470.6:c.1386-3701T>C	ENSP00000409557.2:n.1386-3701T>C
ENST00000460902.2:c.1188T>C	ENSP00000439274.1:n.1188T>C
ENST00000539263.5:c.*876T>C	ENSP00000443245.1:n.*876T>C
NM_003057.2:c.1403T>C	NP_003048.1:p.Val468Ala
NM_153187.1:c.1386-1160T>C	NP_694857.1:n.1386-1160T>C
XM_005267102.3:c.1403T>C	XP_005267159.1:p.Val468Ala
XM_005267103.1:c.1403T>C	XP_005267160.1:p.Val468Ala
XM_005267104.3:c.827T>C	XP_005267161.1:p.Val276Ala
XM_005267105.3:c.827T>C	XP_005267162.1:p.Val276Ala
XM_006715552.1:c.1386-3701T>C	XP_006715615.1:n.1386-3701T>C
XM_011536074.1:c.827T>C	XP_011534376.1:p.Val276Ala
XM_005267102.5:c.1403T>C	XP_005267159.1:p.Val468Ala
XM_005267103.2:c.1403T>C	XP_005267160.1:p.Val468Ala
XM_005267104.5:c.827T>C	XP_005267161.1:p.Val276Ala
XM_005267105.5:c.827T>C	XP_005267162.1:p.Val276Ala
XM_006715552.2:c.1386-3701T>C	XP_006715615.1:n.1386-3701T>C
XM_011536074.3:c.827T>C	XP_011534376.1:p.Val276Ala
NM_003057.3:c.1403T>C MANE Select	NP_003048.1:p.Val468Ala
NM_153187.2:c.1386-1160T>C	NP_694857.1:n.1386-1160T>C