Canonical Allele Identifier: CA350792861
Gene: ABCA12 HGNC NCBI
SNHG31 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214937511_214937513del , CM000664.2:g.214937511_214937513del GRCh38
NC_000002.11:g.215802235_215802237del , CM000664.1:g.215802235_215802237del GRCh37
NC_000002.10:g.215510480_215510482del NCBI36
NG_007074.1:g.205916_205918del

Transcript Alleles

HGVS Amino-acid change
ENST00000272895.12:c.7540_7542del (ABCA12) MANE Select ENSP00000272895.7:p.Lys2514del
ENST00000272895.11:c.7540_7542del (ABCA12) ENSP00000272895.7:p.Lys2514del
ENST00000389661.4:c.6586_6588del (ABCA12) ENSP00000374312.4:p.Lys2196del
NM_015657.3:c.6586_6588del (ABCA12) NP_056472.2:p.Lys2196del
NM_173076.2:c.7540_7542del (ABCA12) NP_775099.2:p.Lys2514del
NR_103740.1:n.7840_7842del (ABCA12)
NR_110292.1:n.322-10314_322-10312del (SNHG31)
XM_011510951.1:c.7549_7551del (ABCA12) XP_011509253.1:p.Lys2517del
XM_011510951.2:c.7549_7551del (ABCA12) XP_011509253.1:p.Lys2517del
NM_173076.3:c.7540_7542del (ABCA12) MANE Select NP_775099.2:p.Lys2514del
NR_103740.2:n.8038_8040del (ABCA12)
NM_015657.4:c.6586_6588del (ABCA12) NP_056472.2:p.Lys2196del