Canonical Allele Identifier: CA361139458

Gene: SLC23A1

Linked Data

• COSMIC: COSM1433464
• MyVariant Identifiers: chr5:g.138715386C>A (hg19) ; chr5:g.139379697C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.139379697C>A , CM000667.2:g.139379697C>A	GRCh38
NC_000005.9:g.138715386C>A , CM000667.1:g.138715386C>A	GRCh37
NC_000005.8:g.138743285C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348729.8:c.906G>T MANE Select	ENSP00000302701.4:p.Trp302Cys
ENST00000348729.7:c.906G>T	ENSP00000302701.4:p.Trp302Cys
ENST00000353963.7:c.918G>T	ENSP00000302851.5:p.Trp306Cys
ENST00000504513.1:c.164+259G>T
ENST00000506512.1:n.517G>T
NM_005847.4:c.906G>T	NP_005838.3:p.Trp302Cys
NM_152685.3:c.918G>T	NP_689898.2:p.Trp306Cys
XM_005272148.3:c.1026G>T	XP_005272205.3:p.Trp342Cys
XM_005272149.3:c.1014G>T	XP_005272206.3:p.Trp338Cys
XM_006714741.2:c.1026G>T	XP_006714804.2:p.Trp342Cys
XM_011543765.1:c.1026G>T	XP_011542067.1:p.Trp342Cys
XM_011543766.1:c.807G>T	XP_011542068.1:p.Trp269Cys
XM_011543767.1:c.711G>T	XP_011542069.1:p.Trp237Cys
XM_011543768.1:c.591G>T	XP_011542070.1:p.Trp197Cys
XM_011543769.1:c.201G>T	XP_011542071.1:p.Trp67Cys
XM_005272149.4:c.1014G>T	XP_005272206.3:p.Trp338Cys
XM_011543765.2:c.1026G>T	XP_011542067.1:p.Trp342Cys
NM_005847.5:c.906G>T MANE Select	NP_005838.3:p.Trp302Cys
NM_152685.4:c.918G>T	NP_689898.2:p.Trp306Cys