Canonical Allele Identifier: CA2662973960

Gene: ABCA12 SNHG31

Linked Data

• gnomAD v4: 2-214932356-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214932356G>T , CM000664.2:g.214932356G>T	GRCh38
NC_000002.11:g.215797080G>T , CM000664.1:g.215797080G>T	GRCh37
NC_000002.10:g.215505325G>T	NCBI36
NG_007074.1:g.211072C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272895.12:c.*278C>A (ABCA12) MANE Select	ENSP00000272895.7:n.*278C>A
ENST00000272895.11:c.*278C>A (ABCA12)	ENSP00000272895.7:n.*278C>A
NM_015657.3:c.*278C>A (ABCA12)	NP_056472.2:n.*278C>A
NM_173076.2:c.*278C>A (ABCA12)	NP_775099.2:n.*278C>A
NR_103740.1:n.8366C>A (ABCA12)
NR_110292.1:n.322-15469G>T (SNHG31)
XM_011510951.1:c.*278C>A (ABCA12)	XP_011509253.1:n.*278C>A
XM_011510951.2:c.*278C>A (ABCA12)	XP_011509253.1:n.*278C>A
NM_173076.3:c.*278C>A (ABCA12) MANE Select	NP_775099.2:n.*278C>A
NR_103740.2:n.8564C>A (ABCA12)
NM_015657.4:c.*278C>A (ABCA12)	NP_056472.2:n.*278C>A