Canonical Allele Identifier: CA2662978482

Gene: ABCA12

Linked Data

• gnomAD v4: 2-214980658-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214980660del , CM000664.2:g.214980660del	GRCh38
NC_000002.11:g.215845384del , CM000664.1:g.215845384del	GRCh37
NC_000002.10:g.215553629del	NCBI36
NG_007074.1:g.162769del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272895.12:c.4580-16del MANE Select	ENSP00000272895.7:n.4580-16del
ENST00000272895.11:c.4580-16del	ENSP00000272895.7:n.4580-16del
ENST00000389661.4:c.3626-16del	ENSP00000374312.4:n.3626-16del
NM_015657.3:c.3626-16del	NP_056472.2:n.3626-16del
NM_173076.2:c.4580-16del	NP_775099.2:n.4580-16del
NR_103740.1:n.4880-16del
XM_011510951.1:c.4589-16del	XP_011509253.1:n.4589-16del
XM_011510952.1:c.4589-16del	XP_011509254.1:n.4589-16del
XM_011510951.2:c.4589-16del	XP_011509253.1:n.4589-16del
NM_173076.3:c.4580-16del MANE Select	NP_775099.2:n.4580-16del
NR_103740.2:n.5078-16del
NM_015657.4:c.3626-16del	NP_056472.2:n.3626-16del