Canonical Allele Identifier: CA2662980586

Gene: ABCA12

Linked Data

• gnomAD v4: 2-215011860-GTGT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215011865_215011867del , CM000664.2:g.215011865_215011867del	GRCh38
NC_000002.11:g.215876589_215876591del , CM000664.1:g.215876589_215876591del	GRCh37
NC_000002.10:g.215584834_215584836del	NCBI36
NG_007074.1:g.131565_131567del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272895.12:c.2121+108_2121+110del MANE Select	ENSP00000272895.7:n.2121+108_2121+110del
ENST00000272895.11:c.2121+108_2121+110del	ENSP00000272895.7:n.2121+108_2121+110del
ENST00000389661.4:c.1167+108_1167+110del	ENSP00000374312.4:n.1167+108_1167+110del
NM_015657.3:c.1167+108_1167+110del	NP_056472.2:n.1167+108_1167+110del
NM_173076.2:c.2121+108_2121+110del	NP_775099.2:n.2121+108_2121+110del
NR_103740.1:n.2365+108_2365+110del
XM_011510951.1:c.2121+108_2121+110del	XP_011509253.1:n.2121+108_2121+110del
XM_011510952.1:c.2121+108_2121+110del	XP_011509254.1:n.2121+108_2121+110del
XM_011510951.2:c.2121+108_2121+110del	XP_011509253.1:n.2121+108_2121+110del
NM_173076.3:c.2121+108_2121+110del MANE Select	NP_775099.2:n.2121+108_2121+110del
NR_103740.2:n.2563+108_2563+110del
NM_015657.4:c.1167+108_1167+110del	NP_056472.2:n.1167+108_1167+110del