Canonical Allele Identifier: CA361139500

Gene: SLC23A1

Linked Data

• MyVariant Identifiers: chr5:g.138715394C>G (hg19) ; chr5:g.139379705C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.139379705C>G , CM000667.2:g.139379705C>G	GRCh38
NC_000005.9:g.138715394C>G , CM000667.1:g.138715394C>G	GRCh37
NC_000005.8:g.138743293C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348729.8:c.898G>C MANE Select	ENSP00000302701.4:p.Ala300Pro
ENST00000348729.7:c.898G>C	ENSP00000302701.4:p.Ala300Pro
ENST00000353963.7:c.910G>C	ENSP00000302851.5:p.Ala304Pro
ENST00000504513.1:c.164+251G>C
ENST00000506512.1:n.509G>C
NM_005847.4:c.898G>C	NP_005838.3:p.Ala300Pro
NM_152685.3:c.910G>C	NP_689898.2:p.Ala304Pro
XM_005272148.3:c.1018G>C	XP_005272205.3:p.Ala340Pro
XM_005272149.3:c.1006G>C	XP_005272206.3:p.Ala336Pro
XM_006714741.2:c.1018G>C	XP_006714804.2:p.Ala340Pro
XM_011543765.1:c.1018G>C	XP_011542067.1:p.Ala340Pro
XM_011543766.1:c.799G>C	XP_011542068.1:p.Ala267Pro
XM_011543767.1:c.703G>C	XP_011542069.1:p.Ala235Pro
XM_011543768.1:c.583G>C	XP_011542070.1:p.Ala195Pro
XM_011543769.1:c.193G>C	XP_011542071.1:p.Ala65Pro
XM_005272149.4:c.1006G>C	XP_005272206.3:p.Ala336Pro
XM_011543765.2:c.1018G>C	XP_011542067.1:p.Ala340Pro
NM_005847.5:c.898G>C MANE Select	NP_005838.3:p.Ala300Pro
NM_152685.4:c.910G>C	NP_689898.2:p.Ala304Pro