Canonical Allele Identifier: CA446793920

Gene: SLC23A1

Linked Data

• MyVariant Identifiers: chr5:g.138715395A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.139379706A>T , CM000667.2:g.139379706A>T	GRCh38
NC_000005.9:g.138715395A>T , CM000667.1:g.138715395A>T	GRCh37
NC_000005.8:g.138743294A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348729.8:c.897T>A MANE Select	ENSP00000302701.4:p.Ile299=
ENST00000348729.7:c.897T>A	ENSP00000302701.4:p.Ile299=
ENST00000353963.7:c.909T>A	ENSP00000302851.5:p.Ile303=
ENST00000504513.1:c.164+250T>A
ENST00000506512.1:n.508T>A
NM_005847.4:c.897T>A	NP_005838.3:p.Ile299=
NM_152685.3:c.909T>A	NP_689898.2:p.Ile303=
XM_005272148.3:c.1017T>A	XP_005272205.3:p.Ile339=
XM_005272149.3:c.1005T>A	XP_005272206.3:p.Ile335=
XM_006714741.2:c.1017T>A	XP_006714804.2:p.Ile339=
XM_011543765.1:c.1017T>A	XP_011542067.1:p.Ile339=
XM_011543766.1:c.798T>A	XP_011542068.1:p.Ile266=
XM_011543767.1:c.702T>A	XP_011542069.1:p.Ile234=
XM_011543768.1:c.582T>A	XP_011542070.1:p.Ile194=
XM_011543769.1:c.192T>A	XP_011542071.1:p.Ile64=
XM_005272149.4:c.1005T>A	XP_005272206.3:p.Ile335=
XM_011543765.2:c.1017T>A	XP_011542067.1:p.Ile339=
NM_005847.5:c.897T>A MANE Select	NP_005838.3:p.Ile299=
NM_152685.4:c.909T>A	NP_689898.2:p.Ile303=