Canonical Allele Identifier: CA361139436

Gene: SLC23A1

Linked Data

• MyVariant Identifiers: chr5:g.138715379T>C (hg19) ; chr5:g.139379690T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.139379690T>C , CM000667.2:g.139379690T>C	GRCh38
NC_000005.9:g.138715379T>C , CM000667.1:g.138715379T>C	GRCh37
NC_000005.8:g.138743278T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348729.8:c.913A>G MANE Select	ENSP00000302701.4:p.Ile305Val
ENST00000348729.7:c.913A>G	ENSP00000302701.4:p.Ile305Val
ENST00000353963.7:c.925A>G	ENSP00000302851.5:p.Ile309Val
ENST00000504513.1:c.164+266A>G
ENST00000506512.1:n.524A>G
NM_005847.4:c.913A>G	NP_005838.3:p.Ile305Val
NM_152685.3:c.925A>G	NP_689898.2:p.Ile309Val
XM_005272148.3:c.1033A>G	XP_005272205.3:p.Ile345Val
XM_005272149.3:c.1021A>G	XP_005272206.3:p.Ile341Val
XM_006714741.2:c.1033A>G	XP_006714804.2:p.Ile345Val
XM_011543765.1:c.1033A>G	XP_011542067.1:p.Ile345Val
XM_011543766.1:c.814A>G	XP_011542068.1:p.Ile272Val
XM_011543767.1:c.718A>G	XP_011542069.1:p.Ile240Val
XM_011543768.1:c.598A>G	XP_011542070.1:p.Ile200Val
XM_011543769.1:c.208A>G	XP_011542071.1:p.Ile70Val
XM_005272149.4:c.1021A>G	XP_005272206.3:p.Ile341Val
XM_011543765.2:c.1033A>G	XP_011542067.1:p.Ile345Val
NM_005847.5:c.913A>G MANE Select	NP_005838.3:p.Ile305Val
NM_152685.4:c.925A>G	NP_689898.2:p.Ile309Val