Canonical Allele Identifier: CA1327140908
Gene: ABCA12 HGNC NCBI
SNHG31 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214932431C= , CM000664.2:g.214932431C= GRCh38
NC_000002.11:g.215797155C= , CM000664.1:g.215797155C= GRCh37
NC_000002.10:g.215505400C= NCBI36
NG_007074.1:g.210997G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000272895.12:c.*203G= (ABCA12) MANE Select ENSP00000272895.7:n.*203G=
ENST00000272895.11:c.*203G= (ABCA12) ENSP00000272895.7:n.*203G=
NM_015657.3:c.*203G= (ABCA12) NP_056472.2:n.*203G=
NM_173076.2:c.*203G= (ABCA12) NP_775099.2:n.*203G=
NR_103740.1:n.8291G= (ABCA12)
NR_110292.1:n.322-15394C= (SNHG31)
XM_011510951.1:c.*203G= (ABCA12) XP_011509253.1:n.*203G=
XM_011510951.2:c.*203G= (ABCA12) XP_011509253.1:n.*203G=
NM_173076.3:c.*203G= (ABCA12) MANE Select NP_775099.2:n.*203G=
NR_103740.2:n.8489G= (ABCA12)
NM_015657.4:c.*203G= (ABCA12) NP_056472.2:n.*203G=
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