Canonical Allele Identifier: CA361140071

Gene: SLC23A1

Linked Data

• MyVariant Identifiers: chr5:g.138715511T>C (hg19) ; chr5:g.139379822T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.139379822T>C , CM000667.2:g.139379822T>C	GRCh38
NC_000005.9:g.138715511T>C , CM000667.1:g.138715511T>C	GRCh37
NC_000005.8:g.138743410T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000348729.8:c.781A>G MANE Select	ENSP00000302701.4:p.Ile261Val
ENST00000348729.7:c.781A>G	ENSP00000302701.4:p.Ile261Val
ENST00000353963.7:c.793A>G	ENSP00000302851.5:p.Ile265Val
ENST00000504513.1:c.164+134A>G
ENST00000506512.1:n.392A>G
NM_005847.4:c.781A>G	NP_005838.3:p.Ile261Val
NM_152685.3:c.793A>G	NP_689898.2:p.Ile265Val
XM_005272148.3:c.901A>G	XP_005272205.3:p.Ile301Val
XM_005272149.3:c.889A>G	XP_005272206.3:p.Ile297Val
XM_006714741.2:c.901A>G	XP_006714804.2:p.Ile301Val
XM_011543765.1:c.901A>G	XP_011542067.1:p.Ile301Val
XM_011543766.1:c.682A>G	XP_011542068.1:p.Ile228Val
XM_011543767.1:c.586A>G	XP_011542069.1:p.Ile196Val
XM_011543768.1:c.466A>G	XP_011542070.1:p.Ile156Val
XM_011543769.1:c.76A>G	XP_011542071.1:p.Ile26Val
XM_005272149.4:c.889A>G	XP_005272206.3:p.Ile297Val
XM_011543765.2:c.901A>G	XP_011542067.1:p.Ile301Val
NM_005847.5:c.781A>G MANE Select	NP_005838.3:p.Ile261Val
NM_152685.4:c.793A>G	NP_689898.2:p.Ile265Val