Canonical Allele Identifier: CA1327160252
Gene: ABCA12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214978650_214978652delinsTCA , CM000664.2:g.214978650_214978652delinsTCA GRCh38
NC_000002.11:g.215843374_215843376delinsTCA , CM000664.1:g.215843374_215843376delinsTCA GRCh37
NC_000002.10:g.215551619_215551621delinsTCA NCBI36
NG_007074.1:g.164776_164778delinsTGA

Transcript Alleles

HGVS Amino-acid change
ENST00000272895.12:c.4977+152_4977+154delinsTGA MANE Select ENSP00000272895.7:n.4977+152_4977+154deli...
ENST00000272895.11:c.4977+152_4977+154delinsTGA ENSP00000272895.7:n.4977+152_4977+154deli...
ENST00000389661.4:c.4023+152_4023+154delinsTGA ENSP00000374312.4:n.4023+152_4023+154deli...
NM_015657.3:c.4023+152_4023+154delinsTGA NP_056472.2:n.4023+152_4023+154delinsTGA
NM_173076.2:c.4977+152_4977+154delinsTGA NP_775099.2:n.4977+152_4977+154delinsTGA
NR_103740.1:n.5277+152_5277+154delinsTGA
XM_011510951.1:c.4986+152_4986+154delinsTGA XP_011509253.1:n.4986+152_4986+154delinsT...
XM_011510952.1:c.4986+152_4986+154delinsTGA XP_011509254.1:n.4986+152_4986+154delinsT...
XM_011510951.2:c.4986+152_4986+154delinsTGA XP_011509253.1:n.4986+152_4986+154delinsT...
NM_173076.3:c.4977+152_4977+154delinsTGA MANE Select NP_775099.2:n.4977+152_4977+154delinsTGA
NR_103740.2:n.5475+152_5475+154delinsTGA
NM_015657.4:c.4023+152_4023+154delinsTGA NP_056472.2:n.4023+152_4023+154delinsTGA