Canonical Allele Identifier: CA647523716

Gene: ABCA12 SNHG31

Linked Data

• COSMIC: COSN23604765

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214932458_214932459insT , CM000664.2:g.214932458_214932459insT	GRCh38
NC_000002.11:g.215797182_215797183insT , CM000664.1:g.215797182_215797183insT	GRCh37
NC_000002.10:g.215505427_215505428insT	NCBI36
NG_007074.1:g.210969_210970insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272895.12:c.*175_*176insA (ABCA12) MANE Select	ENSP00000272895.7:n.*175_*176insA
ENST00000272895.11:c.*175_*176insA (ABCA12)	ENSP00000272895.7:n.*175_*176insA
NM_015657.3:c.*175_*176insA (ABCA12)	NP_056472.2:n.*175_*176insA
NM_173076.2:c.*175_*176insA (ABCA12)	NP_775099.2:n.*175_*176insA
NR_103740.1:n.8263_8264insA (ABCA12)
NR_110292.1:n.322-15367_322-15366insT (SNHG31)
XM_011510951.1:c.*175_*176insA (ABCA12)	XP_011509253.1:n.*175_*176insA
XM_011510951.2:c.*175_*176insA (ABCA12)	XP_011509253.1:n.*175_*176insA
NM_173076.3:c.*175_*176insA (ABCA12) MANE Select	NP_775099.2:n.*175_*176insA
NR_103740.2:n.8461_8462insA (ABCA12)
NM_015657.4:c.*175_*176insA (ABCA12)	NP_056472.2:n.*175_*176insA