Canonical Allele Identifier: CA361139423

Gene: SLC23A1

Linked Data

• MyVariant Identifiers: chr5:g.138715372T>G (hg19) ; chr5:g.139379683T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.139379683T>G , CM000667.2:g.139379683T>G	GRCh38
NC_000005.9:g.138715372T>G , CM000667.1:g.138715372T>G	GRCh37
NC_000005.8:g.138743271T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348729.8:c.920A>C MANE Select	ENSP00000302701.4:p.Tyr307Ser
ENST00000348729.7:c.920A>C	ENSP00000302701.4:p.Tyr307Ser
ENST00000353963.7:c.932A>C	ENSP00000302851.5:p.Tyr311Ser
ENST00000504513.1:c.164+273A>C
ENST00000506512.1:n.531A>C
NM_005847.4:c.920A>C	NP_005838.3:p.Tyr307Ser
NM_152685.3:c.932A>C	NP_689898.2:p.Tyr311Ser
XM_005272148.3:c.1040A>C	XP_005272205.3:p.Tyr347Ser
XM_005272149.3:c.1028A>C	XP_005272206.3:p.Tyr343Ser
XM_006714741.2:c.1040A>C	XP_006714804.2:p.Tyr347Ser
XM_011543765.1:c.1040A>C	XP_011542067.1:p.Tyr347Ser
XM_011543766.1:c.821A>C	XP_011542068.1:p.Tyr274Ser
XM_011543767.1:c.725A>C	XP_011542069.1:p.Tyr242Ser
XM_011543768.1:c.605A>C	XP_011542070.1:p.Tyr202Ser
XM_011543769.1:c.215A>C	XP_011542071.1:p.Tyr72Ser
XM_005272149.4:c.1028A>C	XP_005272206.3:p.Tyr343Ser
XM_011543765.2:c.1040A>C	XP_011542067.1:p.Tyr347Ser
NM_005847.5:c.920A>C MANE Select	NP_005838.3:p.Tyr307Ser
NM_152685.4:c.932A>C	NP_689898.2:p.Tyr311Ser