Canonical Allele Identifier: CA1327140824
Gene: ABCA12 HGNC NCBI
SNHG31 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214932363C= , CM000664.2:g.214932363C= GRCh38
NC_000002.11:g.215797087C= , CM000664.1:g.215797087C= GRCh37
NC_000002.10:g.215505332C= NCBI36
NG_007074.1:g.211065G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000272895.12:c.*271G= (ABCA12) MANE Select ENSP00000272895.7:n.*271G=
ENST00000272895.11:c.*271G= (ABCA12) ENSP00000272895.7:n.*271G=
NM_015657.3:c.*271G= (ABCA12) NP_056472.2:n.*271G=
NM_173076.2:c.*271G= (ABCA12) NP_775099.2:n.*271G=
NR_103740.1:n.8359G= (ABCA12)
NR_110292.1:n.322-15462C= (SNHG31)
XM_011510951.1:c.*271G= (ABCA12) XP_011509253.1:n.*271G=
XM_011510951.2:c.*271G= (ABCA12) XP_011509253.1:n.*271G=
NM_173076.3:c.*271G= (ABCA12) MANE Select NP_775099.2:n.*271G=
NR_103740.2:n.8557G= (ABCA12)
NM_015657.4:c.*271G= (ABCA12) NP_056472.2:n.*271G=
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