Canonical Allele Identifier: CA350447789

Gene: ABCA12

Linked Data

• MyVariant Identifiers: chr2:g.215884420A>T (hg19) ; chr2:g.215019696A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215019696A>T , CM000664.2:g.215019696A>T	GRCh38
NC_000002.11:g.215884420A>T , CM000664.1:g.215884420A>T	GRCh37
NC_000002.10:g.215592665A>T	NCBI36
NG_007074.1:g.123732T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272895.12:c.1388T>A MANE Select	ENSP00000272895.7:p.Leu463Gln
ENST00000272895.11:c.1388T>A	ENSP00000272895.7:p.Leu463Gln
ENST00000389661.4:c.434T>A	ENSP00000374312.4:p.Leu145Gln
NM_015657.3:c.434T>A	NP_056472.2:p.Leu145Gln
NM_173076.2:c.1388T>A	NP_775099.2:p.Leu463Gln
NR_103740.1:n.1632T>A
XM_011510951.1:c.1388T>A	XP_011509253.1:p.Leu463Gln
XM_011510952.1:c.1388T>A	XP_011509254.1:p.Leu463Gln
XM_011510951.2:c.1388T>A	XP_011509253.1:p.Leu463Gln
NM_173076.3:c.1388T>A MANE Select	NP_775099.2:p.Leu463Gln
NR_103740.2:n.1830T>A
NM_015657.4:c.434T>A	NP_056472.2:p.Leu145Gln