Canonical Allele Identifier: CA350792500

Gene: ABCA12 SNHG31

Linked Data

• MyVariant Identifiers: chr2:g.215797454G>C (hg19) ; chr2:g.214932730G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214932730G>C , CM000664.2:g.214932730G>C	GRCh38
NC_000002.11:g.215797454G>C , CM000664.1:g.215797454G>C	GRCh37
NC_000002.10:g.215505699G>C	NCBI36
NG_007074.1:g.210698C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272895.12:c.7692C>G (ABCA12) MANE Select	ENSP00000272895.7:p.Asn2564Lys
ENST00000272895.11:c.7692C>G (ABCA12)	ENSP00000272895.7:p.Asn2564Lys
ENST00000389661.4:c.6738C>G (ABCA12)	ENSP00000374312.4:p.Asn2246Lys
NM_015657.3:c.6738C>G (ABCA12)	NP_056472.2:p.Asn2246Lys
NM_173076.2:c.7692C>G (ABCA12)	NP_775099.2:p.Asn2564Lys
NR_103740.1:n.7992C>G (ABCA12)
NR_110292.1:n.322-15095G>C (SNHG31)
XM_011510951.1:c.7701C>G (ABCA12)	XP_011509253.1:p.Asn2567Lys
XM_011510951.2:c.7701C>G (ABCA12)	XP_011509253.1:p.Asn2567Lys
NM_173076.3:c.7692C>G (ABCA12) MANE Select	NP_775099.2:p.Asn2564Lys
NR_103740.2:n.8190C>G (ABCA12)
NM_015657.4:c.6738C>G (ABCA12)	NP_056472.2:p.Asn2246Lys