Canonical Allele Identifier: CA2347284259

Gene: SLC23A2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.4976975C= , CM000682.2:g.4976975C=	GRCh38
NC_000020.10:g.4957621C= , CM000682.1:g.4957621C=	GRCh37
NC_000020.9:g.4905621C=	NCBI36
NG_029959.1:g.29525G=
NG_029959.2:g.38319G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338244.6:c.-281-6056G= MANE Select	ENSP00000344322.1:n.-281-6056G=
ENST00000338244.5:c.-281-6056G=	ENSP00000344322.1:n.-281-6056G=
ENST00000379333.5:c.-281-6056G=	ENSP00000368637.1:n.-281-6056G=
ENST00000468355.5:n.90-6060G=
NM_005116.5:c.-281-6056G=	NP_005107.4:n.-281-6056G=
NM_203327.1:c.-281-6056G=	NP_976072.1:n.-281-6056G=
XM_011529414.1:c.-277-6060G=	XP_011527716.1:n.-277-6060G=
XM_011529417.1:c.-155+24431G=	XP_011527719.1:n.-155+24431G=
NM_005116.6:c.-281-6056G= MANE Select	NP_005107.4:n.-281-6056G=
NM_203327.2:c.-281-6056G=	NP_976072.1:n.-281-6056G=