Canonical Allele Identifier: CA361140080

Gene: SLC23A1

Linked Data

• MyVariant Identifiers: chr5:g.138715514C>A (hg19) ; chr5:g.139379825C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.139379825C>A , CM000667.2:g.139379825C>A	GRCh38
NC_000005.9:g.138715514C>A , CM000667.1:g.138715514C>A	GRCh37
NC_000005.8:g.138743413C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000348729.8:c.778G>T MANE Select	ENSP00000302701.4:p.Ala260Ser
ENST00000348729.7:c.778G>T	ENSP00000302701.4:p.Ala260Ser
ENST00000353963.7:c.790G>T	ENSP00000302851.5:p.Ala264Ser
ENST00000504513.1:c.164+131G>T
ENST00000506512.1:n.389G>T
NM_005847.4:c.778G>T	NP_005838.3:p.Ala260Ser
NM_152685.3:c.790G>T	NP_689898.2:p.Ala264Ser
XM_005272148.3:c.898G>T	XP_005272205.3:p.Ala300Ser
XM_005272149.3:c.886G>T	XP_005272206.3:p.Ala296Ser
XM_006714741.2:c.898G>T	XP_006714804.2:p.Ala300Ser
XM_011543765.1:c.898G>T	XP_011542067.1:p.Ala300Ser
XM_011543766.1:c.679G>T	XP_011542068.1:p.Ala227Ser
XM_011543767.1:c.583G>T	XP_011542069.1:p.Ala195Ser
XM_011543768.1:c.463G>T	XP_011542070.1:p.Ala155Ser
XM_011543769.1:c.73G>T	XP_011542071.1:p.Ala25Ser
XM_005272149.4:c.886G>T	XP_005272206.3:p.Ala296Ser
XM_011543765.2:c.898G>T	XP_011542067.1:p.Ala300Ser
NM_005847.5:c.778G>T MANE Select	NP_005838.3:p.Ala260Ser
NM_152685.4:c.790G>T	NP_689898.2:p.Ala264Ser