Canonical Allele Identifier: CA361139528

Gene: SLC23A1

Linked Data

• MyVariant Identifiers: chr5:g.138715400C>A (hg19) ; chr5:g.139379711C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.139379711C>A , CM000667.2:g.139379711C>A	GRCh38
NC_000005.9:g.138715400C>A , CM000667.1:g.138715400C>A	GRCh37
NC_000005.8:g.138743299C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348729.8:c.892G>T MANE Select	ENSP00000302701.4:p.Ala298Ser
ENST00000348729.7:c.892G>T	ENSP00000302701.4:p.Ala298Ser
ENST00000353963.7:c.904G>T	ENSP00000302851.5:p.Ala302Ser
ENST00000504513.1:c.164+245G>T
ENST00000506512.1:n.503G>T
NM_005847.4:c.892G>T	NP_005838.3:p.Ala298Ser
NM_152685.3:c.904G>T	NP_689898.2:p.Ala302Ser
XM_005272148.3:c.1012G>T	XP_005272205.3:p.Ala338Ser
XM_005272149.3:c.1000G>T	XP_005272206.3:p.Ala334Ser
XM_006714741.2:c.1012G>T	XP_006714804.2:p.Ala338Ser
XM_011543765.1:c.1012G>T	XP_011542067.1:p.Ala338Ser
XM_011543766.1:c.793G>T	XP_011542068.1:p.Ala265Ser
XM_011543767.1:c.697G>T	XP_011542069.1:p.Ala233Ser
XM_011543768.1:c.577G>T	XP_011542070.1:p.Ala193Ser
XM_011543769.1:c.187G>T	XP_011542071.1:p.Ala63Ser
XM_005272149.4:c.1000G>T	XP_005272206.3:p.Ala334Ser
XM_011543765.2:c.1012G>T	XP_011542067.1:p.Ala338Ser
NM_005847.5:c.892G>T MANE Select	NP_005838.3:p.Ala298Ser
NM_152685.4:c.904G>T	NP_689898.2:p.Ala302Ser