Canonical Allele Identifier: CA361139853

Gene: SLC23A1

Linked Data

• MyVariant Identifiers: chr5:g.138715477G>T (hg19) ; chr5:g.139379788G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.139379788G>T , CM000667.2:g.139379788G>T	GRCh38
NC_000005.9:g.138715477G>T , CM000667.1:g.138715477G>T	GRCh37
NC_000005.8:g.138743376G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348729.8:c.815C>A MANE Select	ENSP00000302701.4:p.Thr272Asn
ENST00000348729.7:c.815C>A	ENSP00000302701.4:p.Thr272Asn
ENST00000353963.7:c.827C>A	ENSP00000302851.5:p.Thr276Asn
ENST00000504513.1:c.164+168C>A
ENST00000506512.1:n.426C>A
NM_005847.4:c.815C>A	NP_005838.3:p.Thr272Asn
NM_152685.3:c.827C>A	NP_689898.2:p.Thr276Asn
XM_005272148.3:c.935C>A	XP_005272205.3:p.Thr312Asn
XM_005272149.3:c.923C>A	XP_005272206.3:p.Thr308Asn
XM_006714741.2:c.935C>A	XP_006714804.2:p.Thr312Asn
XM_011543765.1:c.935C>A	XP_011542067.1:p.Thr312Asn
XM_011543766.1:c.716C>A	XP_011542068.1:p.Thr239Asn
XM_011543767.1:c.620C>A	XP_011542069.1:p.Thr207Asn
XM_011543768.1:c.500C>A	XP_011542070.1:p.Thr167Asn
XM_011543769.1:c.110C>A	XP_011542071.1:p.Thr37Asn
XM_005272149.4:c.923C>A	XP_005272206.3:p.Thr308Asn
XM_011543765.2:c.935C>A	XP_011542067.1:p.Thr312Asn
NM_005847.5:c.815C>A MANE Select	NP_005838.3:p.Thr272Asn
NM_152685.4:c.827C>A	NP_689898.2:p.Thr276Asn