Canonical Allele Identifier: CA2347284302
Gene: SLC23A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.4977085G= , CM000682.2:g.4977085G= GRCh38
NC_000020.10:g.4957731G= , CM000682.1:g.4957731G= GRCh37
NC_000020.9:g.4905731G= NCBI36
NG_029959.1:g.29415C=
NG_029959.2:g.38209C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000338244.6:c.-281-6166C= MANE Select ENSP00000344322.1:n.-281-6166C=
ENST00000338244.5:c.-281-6166C= ENSP00000344322.1:n.-281-6166C=
ENST00000379333.5:c.-281-6166C= ENSP00000368637.1:n.-281-6166C=
ENST00000468355.5:n.90-6170C=
NM_005116.5:c.-281-6166C= NP_005107.4:n.-281-6166C=
NM_203327.1:c.-281-6166C= NP_976072.1:n.-281-6166C=
XM_011529414.1:c.-277-6170C= XP_011527716.1:n.-277-6170C=
XM_011529417.1:c.-155+24321C= XP_011527719.1:n.-155+24321C=
NM_005116.6:c.-281-6166C= MANE Select NP_005107.4:n.-281-6166C=
NM_203327.2:c.-281-6166C= NP_976072.1:n.-281-6166C=