Canonical Allele Identifier: CA2347284289
Gene: SLC23A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.4977054T= , CM000682.2:g.4977054T= GRCh38
NC_000020.10:g.4957700T= , CM000682.1:g.4957700T= GRCh37
NC_000020.9:g.4905700T= NCBI36
NG_029959.1:g.29446A=
NG_029959.2:g.38240A=

Transcript Alleles

HGVS Amino-acid Change
NM_005116.6:c.-281-6135A= MANE Select NP_005107.4:n.-281-6135A=
ENST00000338244.6:c.-281-6135A= MANE Select ENSP00000344322.1:n.-281-6135A=
NM_005116.5:c.-281-6135A= NP_005107.4:n.-281-6135A=
NM_203327.1:c.-281-6135A= NP_976072.1:n.-281-6135A=
NM_203327.2:c.-281-6135A= NP_976072.1:n.-281-6135A=
ENST00000338244.5:c.-281-6135A= ENSP00000344322.1:n.-281-6135A=
ENST00000379333.5:c.-281-6135A= ENSP00000368637.1:n.-281-6135A=
ENST00000468355.5:n.90-6139A=
XM_011529414.1:c.-277-6139A= XP_011527716.1:n.-277-6139A=
XM_011529417.1:c.-155+24352A= XP_011527719.1:n.-155+24352A=