Canonical Allele Identifier: CA361139507

Gene: SLC23A1

Linked Data

• MyVariant Identifiers: chr5:g.138715396A>C (hg19) ; chr5:g.139379707A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.139379707A>C , CM000667.2:g.139379707A>C	GRCh38
NC_000005.9:g.138715396A>C , CM000667.1:g.138715396A>C	GRCh37
NC_000005.8:g.138743295A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348729.8:c.896T>G MANE Select	ENSP00000302701.4:p.Ile299Ser
ENST00000348729.7:c.896T>G	ENSP00000302701.4:p.Ile299Ser
ENST00000353963.7:c.908T>G	ENSP00000302851.5:p.Ile303Ser
ENST00000504513.1:c.164+249T>G
ENST00000506512.1:n.507T>G
NM_005847.4:c.896T>G	NP_005838.3:p.Ile299Ser
NM_152685.3:c.908T>G	NP_689898.2:p.Ile303Ser
XM_005272148.3:c.1016T>G	XP_005272205.3:p.Ile339Ser
XM_005272149.3:c.1004T>G	XP_005272206.3:p.Ile335Ser
XM_006714741.2:c.1016T>G	XP_006714804.2:p.Ile339Ser
XM_011543765.1:c.1016T>G	XP_011542067.1:p.Ile339Ser
XM_011543766.1:c.797T>G	XP_011542068.1:p.Ile266Ser
XM_011543767.1:c.701T>G	XP_011542069.1:p.Ile234Ser
XM_011543768.1:c.581T>G	XP_011542070.1:p.Ile194Ser
XM_011543769.1:c.191T>G	XP_011542071.1:p.Ile64Ser
XM_005272149.4:c.1004T>G	XP_005272206.3:p.Ile335Ser
XM_011543765.2:c.1016T>G	XP_011542067.1:p.Ile339Ser
NM_005847.5:c.896T>G MANE Select	NP_005838.3:p.Ile299Ser
NM_152685.4:c.908T>G	NP_689898.2:p.Ile303Ser