Canonical Allele Identifier: CA539837718

Gene: ABCA12

Linked Data

• gnomAD v2: 2-215876538-ATT-A
• MyVariant Identifiers: chr2:g.215876539_215876540del (hg19) ; chr2:g.215011815_215011816del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215011815_215011816del , CM000664.2:g.215011815_215011816del	GRCh38
NC_000002.11:g.215876539_215876540del , CM000664.1:g.215876539_215876540del	GRCh37
NC_000002.10:g.215584784_215584785del	NCBI36
NG_007074.1:g.131612_131613del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272895.12:c.2121+155_2121+156del MANE Select	ENSP00000272895.7:n.2121+155_2121+156del
ENST00000272895.11:c.2121+155_2121+156del	ENSP00000272895.7:n.2121+155_2121+156del
ENST00000389661.4:c.1167+155_1167+156del	ENSP00000374312.4:n.1167+155_1167+156del
NM_015657.3:c.1167+155_1167+156del	NP_056472.2:n.1167+155_1167+156del
NM_173076.2:c.2121+155_2121+156del	NP_775099.2:n.2121+155_2121+156del
NR_103740.1:n.2365+155_2365+156del
XM_011510951.1:c.2121+155_2121+156del	XP_011509253.1:n.2121+155_2121+156del
XM_011510952.1:c.2121+155_2121+156del	XP_011509254.1:n.2121+155_2121+156del
XM_011510951.2:c.2121+155_2121+156del	XP_011509253.1:n.2121+155_2121+156del
NM_173076.3:c.2121+155_2121+156del MANE Select	NP_775099.2:n.2121+155_2121+156del
NR_103740.2:n.2563+155_2563+156del
NM_015657.4:c.1167+155_1167+156del	NP_056472.2:n.1167+155_1167+156del