Canonical Allele Identifier: CA350483391

Gene: ABCA12

Linked Data

• MyVariant Identifiers: chr2:g.215876168T>G (hg19) ; chr2:g.215011444T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215011444T>G , CM000664.2:g.215011444T>G	GRCh38
NC_000002.11:g.215876168T>G , CM000664.1:g.215876168T>G	GRCh37
NC_000002.10:g.215584413T>G	NCBI36
NG_007074.1:g.131984A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000272895.12:c.2327A>C MANE Select	ENSP00000272895.7:p.Asn776Thr
ENST00000272895.11:c.2327A>C	ENSP00000272895.7:p.Asn776Thr
ENST00000389661.4:c.1373A>C	ENSP00000374312.4:p.Asn458Thr
NM_015657.3:c.1373A>C	NP_056472.2:p.Asn458Thr
NM_173076.2:c.2327A>C	NP_775099.2:p.Asn776Thr
NR_103740.1:n.2571A>C
XM_011510951.1:c.2327A>C	XP_011509253.1:p.Asn776Thr
XM_011510952.1:c.2327A>C	XP_011509254.1:p.Asn776Thr
XM_011510951.2:c.2327A>C	XP_011509253.1:p.Asn776Thr
NM_173076.3:c.2327A>C MANE Select	NP_775099.2:p.Asn776Thr
NR_103740.2:n.2769A>C
NM_015657.4:c.1373A>C	NP_056472.2:p.Asn458Thr