Canonical Allele Identifier: CA1042213950

Gene: ABCA12

Linked Data

• gnomAD v3: 2-215011885-A-T
• gnomAD v4: 2-215011885-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215011885A>T , CM000664.2:g.215011885A>T	GRCh38
NC_000002.11:g.215876609A>T , CM000664.1:g.215876609A>T	GRCh37
NC_000002.10:g.215584854A>T	NCBI36
NG_007074.1:g.131543T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272895.12:c.2121+86T>A MANE Select	ENSP00000272895.7:n.2121+86T>A
ENST00000272895.11:c.2121+86T>A	ENSP00000272895.7:n.2121+86T>A
ENST00000389661.4:c.1167+86T>A	ENSP00000374312.4:n.1167+86T>A
NM_015657.3:c.1167+86T>A	NP_056472.2:n.1167+86T>A
NM_173076.2:c.2121+86T>A	NP_775099.2:n.2121+86T>A
NR_103740.1:n.2365+86T>A
XM_011510951.1:c.2121+86T>A	XP_011509253.1:n.2121+86T>A
XM_011510952.1:c.2121+86T>A	XP_011509254.1:n.2121+86T>A
XM_011510951.2:c.2121+86T>A	XP_011509253.1:n.2121+86T>A
NM_173076.3:c.2121+86T>A MANE Select	NP_775099.2:n.2121+86T>A
NR_103740.2:n.2563+86T>A
NM_015657.4:c.1167+86T>A	NP_056472.2:n.1167+86T>A