Canonical Allele Identifier: CA1327140470
Gene: ABCA12 HGNC NCBI
SNHG31 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214932764G= , CM000664.2:g.214932764G= GRCh38
NC_000002.11:g.215797488G= , CM000664.1:g.215797488G= GRCh37
NC_000002.10:g.215505733G= NCBI36
NG_007074.1:g.210664C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000272895.12:c.7681-23C= (ABCA12) MANE Select ENSP00000272895.7:n.7681-23C=
ENST00000272895.11:c.7681-23C= (ABCA12) ENSP00000272895.7:n.7681-23C=
ENST00000389661.4:c.6727-23C= (ABCA12) ENSP00000374312.4:n.6727-23C=
NM_015657.3:c.6727-23C= (ABCA12) NP_056472.2:n.6727-23C=
NM_173076.2:c.7681-23C= (ABCA12) NP_775099.2:n.7681-23C=
NR_103740.1:n.7981-23C= (ABCA12)
NR_110292.1:n.322-15061G= (SNHG31)
XM_011510951.1:c.7690-23C= (ABCA12) XP_011509253.1:n.7690-23C=
XM_011510951.2:c.7690-23C= (ABCA12) XP_011509253.1:n.7690-23C=
NM_173076.3:c.7681-23C= (ABCA12) MANE Select NP_775099.2:n.7681-23C=
NR_103740.2:n.8179-23C= (ABCA12)
NM_015657.4:c.6727-23C= (ABCA12) NP_056472.2:n.6727-23C=
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