Canonical Allele Identifier: CA350792870

Gene: ABCA12 SNHG31

Linked Data

• gnomAD v4: 2-214937514-A-G
• MyVariant Identifiers: chr2:g.215802238A>G (hg19) ; chr2:g.214937514A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214937514A>G , CM000664.2:g.214937514A>G	GRCh38
NC_000002.11:g.215802238A>G , CM000664.1:g.215802238A>G	GRCh37
NC_000002.10:g.215510483A>G	NCBI36
NG_007074.1:g.205914T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272895.12:c.7538T>C (ABCA12) MANE Select	ENSP00000272895.7:p.Leu2513Ser
ENST00000272895.11:c.7538T>C (ABCA12)	ENSP00000272895.7:p.Leu2513Ser
ENST00000389661.4:c.6584T>C (ABCA12)	ENSP00000374312.4:p.Leu2195Ser
NM_015657.3:c.6584T>C (ABCA12)	NP_056472.2:p.Leu2195Ser
NM_173076.2:c.7538T>C (ABCA12)	NP_775099.2:p.Leu2513Ser
NR_103740.1:n.7838T>C (ABCA12)
NR_110292.1:n.322-10311A>G (SNHG31)
XM_011510951.1:c.7547T>C (ABCA12)	XP_011509253.1:p.Leu2516Ser
XM_011510951.2:c.7547T>C (ABCA12)	XP_011509253.1:p.Leu2516Ser
NM_173076.3:c.7538T>C (ABCA12) MANE Select	NP_775099.2:p.Leu2513Ser
NR_103740.2:n.8036T>C (ABCA12)
NM_015657.4:c.6584T>C (ABCA12)	NP_056472.2:p.Leu2195Ser