Canonical Allele Identifier: CA2347284309
Gene: SLC23A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.4977114C= , CM000682.2:g.4977114C= GRCh38
NC_000020.10:g.4957760C= , CM000682.1:g.4957760C= GRCh37
NC_000020.9:g.4905760C= NCBI36
NG_029959.1:g.29386G=
NG_029959.2:g.38180G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000338244.6:c.-281-6195G= MANE Select ENSP00000344322.1:n.-281-6195G=
ENST00000338244.5:c.-281-6195G= ENSP00000344322.1:n.-281-6195G=
ENST00000379333.5:c.-281-6195G= ENSP00000368637.1:n.-281-6195G=
ENST00000468355.5:n.90-6199G=
NM_005116.5:c.-281-6195G= NP_005107.4:n.-281-6195G=
NM_203327.1:c.-281-6195G= NP_976072.1:n.-281-6195G=
XM_011529414.1:c.-277-6199G= XP_011527716.1:n.-277-6199G=
XM_011529417.1:c.-155+24292G= XP_011527719.1:n.-155+24292G=
NM_005116.6:c.-281-6195G= MANE Select NP_005107.4:n.-281-6195G=
NM_203327.2:c.-281-6195G= NP_976072.1:n.-281-6195G=
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