Canonical Allele Identifier: CA361139659

Gene: SLC23A1

Linked Data

• dbSNP Id: rs1243048496
• gnomAD v4: 5-139379737-C-T
• MyVariant Identifiers: chr5:g.138715426C>T (hg19) ; chr5:g.139379737C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.139379737C>T , CM000667.2:g.139379737C>T	GRCh38
NC_000005.9:g.138715426C>T , CM000667.1:g.138715426C>T	GRCh37
NC_000005.8:g.138743325C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348729.8:c.866G>A MANE Select	ENSP00000302701.4:p.Arg289Gln
ENST00000348729.7:c.866G>A	ENSP00000302701.4:p.Arg289Gln
ENST00000353963.7:c.878G>A	ENSP00000302851.5:p.Arg293Gln
ENST00000504513.1:c.164+219G>A
ENST00000506512.1:n.477G>A
NM_005847.4:c.866G>A	NP_005838.3:p.Arg289Gln
NM_152685.3:c.878G>A	NP_689898.2:p.Arg293Gln
XM_005272148.3:c.986G>A	XP_005272205.3:p.Arg329Gln
XM_005272149.3:c.974G>A	XP_005272206.3:p.Arg325Gln
XM_006714741.2:c.986G>A	XP_006714804.2:p.Arg329Gln
XM_011543765.1:c.986G>A	XP_011542067.1:p.Arg329Gln
XM_011543766.1:c.767G>A	XP_011542068.1:p.Arg256Gln
XM_011543767.1:c.671G>A	XP_011542069.1:p.Arg224Gln
XM_011543768.1:c.551G>A	XP_011542070.1:p.Arg184Gln
XM_011543769.1:c.161G>A	XP_011542071.1:p.Arg54Gln
XM_005272149.4:c.974G>A	XP_005272206.3:p.Arg325Gln
XM_011543765.2:c.986G>A	XP_011542067.1:p.Arg329Gln
NM_005847.5:c.866G>A MANE Select	NP_005838.3:p.Arg289Gln
NM_152685.4:c.878G>A	NP_689898.2:p.Arg293Gln