Canonical Allele Identifier: CA2662975041

Gene: ABCA12 SNHG31

Linked Data

• gnomAD v4: 2-214947394-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214947394T>C , CM000664.2:g.214947394T>C	GRCh38
NC_000002.11:g.215812118T>C , CM000664.1:g.215812118T>C	GRCh37
NC_000002.10:g.215520363T>C	NCBI36
NG_007074.1:g.196034A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000272895.12:c.7239+28A>G (ABCA12) MANE Select	ENSP00000272895.7:n.7239+28A>G
ENST00000272895.11:c.7239+28A>G (ABCA12)	ENSP00000272895.7:n.7239+28A>G
ENST00000389661.4:c.6285+28A>G (ABCA12)	ENSP00000374312.4:n.6285+28A>G
NM_015657.3:c.6285+28A>G (ABCA12)	NP_056472.2:n.6285+28A>G
NM_173076.2:c.7239+28A>G (ABCA12)	NP_775099.2:n.7239+28A>G
NR_103740.1:n.7539+28A>G (ABCA12)
NR_110292.1:n.322-431T>C (SNHG31)
XM_011510951.1:c.7248+28A>G (ABCA12)	XP_011509253.1:n.7248+28A>G
XM_011510951.2:c.7248+28A>G (ABCA12)	XP_011509253.1:n.7248+28A>G
NM_173076.3:c.7239+28A>G (ABCA12) MANE Select	NP_775099.2:n.7239+28A>G
NR_103740.2:n.7737+28A>G (ABCA12)
NM_015657.4:c.6285+28A>G (ABCA12)	NP_056472.2:n.6285+28A>G