Canonical Allele Identifier: CA350461048

Gene: ABCA12

Linked Data

• gnomAD v4: 2-214980580-G-T
• MyVariant Identifiers: chr2:g.215845304G>T (hg19) ; chr2:g.214980580G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214980580G>T , CM000664.2:g.214980580G>T	GRCh38
NC_000002.11:g.215845304G>T , CM000664.1:g.215845304G>T	GRCh37
NC_000002.10:g.215553549G>T	NCBI36
NG_007074.1:g.162848C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272895.12:c.4643C>A MANE Select	ENSP00000272895.7:p.Ala1548Asp
ENST00000272895.11:c.4643C>A	ENSP00000272895.7:p.Ala1548Asp
ENST00000389661.4:c.3689C>A	ENSP00000374312.4:p.Ala1230Asp
NM_015657.3:c.3689C>A	NP_056472.2:p.Ala1230Asp
NM_173076.2:c.4643C>A	NP_775099.2:p.Ala1548Asp
NR_103740.1:n.4943C>A
XM_011510951.1:c.4652C>A	XP_011509253.1:p.Ala1551Asp
XM_011510952.1:c.4652C>A	XP_011509254.1:p.Ala1551Asp
XM_011510951.2:c.4652C>A	XP_011509253.1:p.Ala1551Asp
NM_173076.3:c.4643C>A MANE Select	NP_775099.2:p.Ala1548Asp
NR_103740.2:n.5141C>A
NM_015657.4:c.3689C>A	NP_056472.2:p.Ala1230Asp