Canonical Allele Identifier: CA2347284261
Gene: SLC23A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.4976977A= , CM000682.2:g.4976977A= GRCh38
NC_000020.10:g.4957623A= , CM000682.1:g.4957623A= GRCh37
NC_000020.9:g.4905623A= NCBI36
NG_029959.1:g.29523T=
NG_029959.2:g.38317T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000338244.6:c.-281-6058T= MANE Select ENSP00000344322.1:n.-281-6058T=
ENST00000338244.5:c.-281-6058T= ENSP00000344322.1:n.-281-6058T=
ENST00000379333.5:c.-281-6058T= ENSP00000368637.1:n.-281-6058T=
ENST00000468355.5:n.90-6062T=
NM_005116.5:c.-281-6058T= NP_005107.4:n.-281-6058T=
NM_203327.1:c.-281-6058T= NP_976072.1:n.-281-6058T=
XM_011529414.1:c.-277-6062T= XP_011527716.1:n.-277-6062T=
XM_011529417.1:c.-155+24429T= XP_011527719.1:n.-155+24429T=
NM_005116.6:c.-281-6058T= MANE Select NP_005107.4:n.-281-6058T=
NM_203327.2:c.-281-6058T= NP_976072.1:n.-281-6058T=