Canonical Allele Identifier: CA350459636

Gene: ABCA12

Linked Data

• MyVariant Identifiers: chr2:g.215843568T>C (hg19) ; chr2:g.214978844T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214978844T>C , CM000664.2:g.214978844T>C	GRCh38
NC_000002.11:g.215843568T>C , CM000664.1:g.215843568T>C	GRCh37
NC_000002.10:g.215551813T>C	NCBI36
NG_007074.1:g.164584A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000272895.12:c.4937A>G MANE Select	ENSP00000272895.7:p.Asn1646Ser
ENST00000272895.11:c.4937A>G	ENSP00000272895.7:p.Asn1646Ser
ENST00000389661.4:c.3983A>G	ENSP00000374312.4:p.Asn1328Ser
NM_015657.3:c.3983A>G	NP_056472.2:p.Asn1328Ser
NM_173076.2:c.4937A>G	NP_775099.2:p.Asn1646Ser
NR_103740.1:n.5237A>G
XM_011510951.1:c.4946A>G	XP_011509253.1:p.Asn1649Ser
XM_011510952.1:c.4946A>G	XP_011509254.1:p.Asn1649Ser
XM_011510951.2:c.4946A>G	XP_011509253.1:p.Asn1649Ser
NM_173076.3:c.4937A>G MANE Select	NP_775099.2:p.Asn1646Ser
NR_103740.2:n.5435A>G
NM_015657.4:c.3983A>G	NP_056472.2:p.Asn1328Ser