Canonical Allele Identifier: CA2662980259

Gene: ABCA12

Linked Data

• gnomAD v4: 2-215011381-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215011381G>C , CM000664.2:g.215011381G>C	GRCh38
NC_000002.11:g.215876105G>C , CM000664.1:g.215876105G>C	GRCh37
NC_000002.10:g.215584350G>C	NCBI36
NG_007074.1:g.132047C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000272895.12:c.2332+58C>G MANE Select	ENSP00000272895.7:n.2332+58C>G
ENST00000272895.11:c.2332+58C>G	ENSP00000272895.7:n.2332+58C>G
ENST00000389661.4:c.1378+58C>G	ENSP00000374312.4:n.1378+58C>G
NM_015657.3:c.1378+58C>G	NP_056472.2:n.1378+58C>G
NM_173076.2:c.2332+58C>G	NP_775099.2:n.2332+58C>G
NR_103740.1:n.2576+58C>G
XM_011510951.1:c.2332+58C>G	XP_011509253.1:n.2332+58C>G
XM_011510952.1:c.2332+58C>G	XP_011509254.1:n.2332+58C>G
XM_011510951.2:c.2332+58C>G	XP_011509253.1:n.2332+58C>G
NM_173076.3:c.2332+58C>G MANE Select	NP_775099.2:n.2332+58C>G
NR_103740.2:n.2774+58C>G
NM_015657.4:c.1378+58C>G	NP_056472.2:n.1378+58C>G