Canonical Allele Identifier: CA2347254857

Gene: SLC23A2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.4911007T= , CM000682.2:g.4911007T=	GRCh38
NC_000020.10:g.4891653T= , CM000682.1:g.4891653T=	GRCh37
NC_000020.9:g.4839653T=	NCBI36
NG_029959.1:g.95493A=
NG_029959.2:g.104287A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000338244.6:c.207+1873A= MANE Select	ENSP00000344322.1:n.207+1873A=
ENST00000338244.5:c.207+1873A=	ENSP00000344322.1:n.207+1873A=
ENST00000379333.5:c.207+1873A=	ENSP00000368637.1:n.207+1873A=
ENST00000468355.5:n.573+1873A=
NM_005116.5:c.207+1873A=	NP_005107.4:n.207+1873A=
NM_203327.1:c.207+1873A=	NP_976072.1:n.207+1873A=
XM_011529414.1:c.207+1873A=	XP_011527716.1:n.207+1873A=
XM_011529415.1:c.207+1873A=	XP_011527717.1:n.207+1873A=
XM_011529416.1:c.207+1873A=	XP_011527718.1:n.207+1873A=
XM_011529417.1:c.207+1873A=	XP_011527719.1:n.207+1873A=
NM_005116.6:c.207+1873A= MANE Select	NP_005107.4:n.207+1873A=
NM_203327.2:c.207+1873A=	NP_976072.1:n.207+1873A=