Canonical Allele Identifier: CA2347284251

Gene: SLC23A2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.4976958T= , CM000682.2:g.4976958T=	GRCh38
NC_000020.10:g.4957604T= , CM000682.1:g.4957604T=	GRCh37
NC_000020.9:g.4905604T=	NCBI36
NG_029959.1:g.29542A=
NG_029959.2:g.38336A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338244.6:c.-281-6039A= MANE Select	ENSP00000344322.1:n.-281-6039A=
ENST00000338244.5:c.-281-6039A=	ENSP00000344322.1:n.-281-6039A=
ENST00000379333.5:c.-281-6039A=	ENSP00000368637.1:n.-281-6039A=
ENST00000468355.5:n.90-6043A=
NM_005116.5:c.-281-6039A=	NP_005107.4:n.-281-6039A=
NM_203327.1:c.-281-6039A=	NP_976072.1:n.-281-6039A=
XM_011529414.1:c.-277-6043A=	XP_011527716.1:n.-277-6043A=
XM_011529417.1:c.-155+24448A=	XP_011527719.1:n.-155+24448A=
NM_005116.6:c.-281-6039A= MANE Select	NP_005107.4:n.-281-6039A=
NM_203327.2:c.-281-6039A=	NP_976072.1:n.-281-6039A=