Canonical Allele Identifier: CA350461225

Gene: ABCA12

Linked Data

• COSMIC: COSM6377751 ; COSM6377752
• MyVariant Identifiers: chr2:g.215845346G>T (hg19) ; chr2:g.214980622G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214980622G>T , CM000664.2:g.214980622G>T	GRCh38
NC_000002.11:g.215845346G>T , CM000664.1:g.215845346G>T	GRCh37
NC_000002.10:g.215553591G>T	NCBI36
NG_007074.1:g.162806C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272895.12:c.4601C>A MANE Select	ENSP00000272895.7:p.Thr1534Lys
ENST00000272895.11:c.4601C>A	ENSP00000272895.7:p.Thr1534Lys
ENST00000389661.4:c.3647C>A	ENSP00000374312.4:p.Thr1216Lys
NM_015657.3:c.3647C>A	NP_056472.2:p.Thr1216Lys
NM_173076.2:c.4601C>A	NP_775099.2:p.Thr1534Lys
NR_103740.1:n.4901C>A
XM_011510951.1:c.4610C>A	XP_011509253.1:p.Thr1537Lys
XM_011510952.1:c.4610C>A	XP_011509254.1:p.Thr1537Lys
XM_011510951.2:c.4610C>A	XP_011509253.1:p.Thr1537Lys
NM_173076.3:c.4601C>A MANE Select	NP_775099.2:p.Thr1534Lys
NR_103740.2:n.5099C>A
NM_015657.4:c.3647C>A	NP_056472.2:p.Thr1216Lys