Canonical Allele Identifier: CA361139473

Gene: SLC23A1

Linked Data

• dbSNP Id: rs1454742629
• gnomAD v3: 5-139379699-A-G
• gnomAD v4: 5-139379699-A-G
• MyVariant Identifiers: chr5:g.138715388A>G (hg19) ; chr5:g.139379699A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.139379699A>G , CM000667.2:g.139379699A>G	GRCh38
NC_000005.9:g.138715388A>G , CM000667.1:g.138715388A>G	GRCh37
NC_000005.8:g.138743287A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348729.8:c.904T>C MANE Select	ENSP00000302701.4:p.Trp302Arg
ENST00000348729.7:c.904T>C	ENSP00000302701.4:p.Trp302Arg
ENST00000353963.7:c.916T>C	ENSP00000302851.5:p.Trp306Arg
ENST00000504513.1:c.164+257T>C
ENST00000506512.1:n.515T>C
NM_005847.4:c.904T>C	NP_005838.3:p.Trp302Arg
NM_152685.3:c.916T>C	NP_689898.2:p.Trp306Arg
XM_005272148.3:c.1024T>C	XP_005272205.3:p.Trp342Arg
XM_005272149.3:c.1012T>C	XP_005272206.3:p.Trp338Arg
XM_006714741.2:c.1024T>C	XP_006714804.2:p.Trp342Arg
XM_011543765.1:c.1024T>C	XP_011542067.1:p.Trp342Arg
XM_011543766.1:c.805T>C	XP_011542068.1:p.Trp269Arg
XM_011543767.1:c.709T>C	XP_011542069.1:p.Trp237Arg
XM_011543768.1:c.589T>C	XP_011542070.1:p.Trp197Arg
XM_011543769.1:c.199T>C	XP_011542071.1:p.Trp67Arg
XM_005272149.4:c.1012T>C	XP_005272206.3:p.Trp338Arg
XM_011543765.2:c.1024T>C	XP_011542067.1:p.Trp342Arg
NM_005847.5:c.904T>C MANE Select	NP_005838.3:p.Trp302Arg
NM_152685.4:c.916T>C	NP_689898.2:p.Trp306Arg