Canonical Allele Identifier: CA2555780042
Gene: SLC23A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.4976972T>G , CM000682.2:g.4976972T>G GRCh38
NC_000020.10:g.4957618T>G , CM000682.1:g.4957618T>G GRCh37
NC_000020.9:g.4905618T>G NCBI36
NG_029959.1:g.29528A>C
NG_029959.2:g.38322A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000338244.6:c.-281-6053A>C MANE Select ENSP00000344322.1:n.-281-6053A>C
ENST00000338244.5:c.-281-6053A>C ENSP00000344322.1:n.-281-6053A>C
ENST00000379333.5:c.-281-6053A>C ENSP00000368637.1:n.-281-6053A>C
ENST00000468355.5:n.90-6057A>C
NM_005116.5:c.-281-6053A>C NP_005107.4:n.-281-6053A>C
NM_203327.1:c.-281-6053A>C NP_976072.1:n.-281-6053A>C
XM_011529414.1:c.-277-6057A>C XP_011527716.1:n.-277-6057A>C
XM_011529417.1:c.-155+24434A>C XP_011527719.1:n.-155+24434A>C
NM_005116.6:c.-281-6053A>C MANE Select NP_005107.4:n.-281-6053A>C
NM_203327.2:c.-281-6053A>C NP_976072.1:n.-281-6053A>C