Canonical Allele Identifier: CA1327140799

Gene: ABCA12 SNHG31

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214932335_214932340delinsATAAAT , CM000664.2:g.214932335_214932340delinsATAAAT	GRCh38
NC_000002.11:g.215797059_215797064delinsATAAAT , CM000664.1:g.215797059_215797064delinsATAAAT	GRCh37
NC_000002.10:g.215505304_215505309delinsATAAAT	NCBI36
NG_007074.1:g.211088_211093delinsATTTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272895.12:c.*294_*299delinsATTTAT (ABCA12) MANE Select	ENSP00000272895.7:n.*294_*299delinsATTTAT
ENST00000272895.11:c.*294_*299delinsATTTAT (ABCA12)	ENSP00000272895.7:n.*294_*299delinsATTTAT
NM_015657.3:c.*294_*299delinsATTTAT (ABCA12)	NP_056472.2:n.*294_*299delinsATTTAT
NM_173076.2:c.*294_*299delinsATTTAT (ABCA12)	NP_775099.2:n.*294_*299delinsATTTAT
NR_103740.1:n.8382_8387delinsATTTAT (ABCA12)
NR_110292.1:n.322-15490_322-15485delinsATAAAT (SNHG31)
XM_011510951.1:c.*294_*299delinsATTTAT (ABCA12)	XP_011509253.1:n.*294_*299delinsATTTAT
XM_011510951.2:c.*294_*299delinsATTTAT (ABCA12)	XP_011509253.1:n.*294_*299delinsATTTAT
NM_173076.3:c.*294_*299delinsATTTAT (ABCA12) MANE Select	NP_775099.2:n.*294_*299delinsATTTAT
NR_103740.2:n.8580_8585delinsATTTAT (ABCA12)
NM_015657.4:c.*294_*299delinsATTTAT (ABCA12)	NP_056472.2:n.*294_*299delinsATTTAT