Canonical Allele Identifier: CA1327155420
Gene: ABCA12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214966975C= , CM000664.2:g.214966975C= GRCh38
NC_000002.11:g.215831699C= , CM000664.1:g.215831699C= GRCh37
NC_000002.10:g.215539944C= NCBI36
NG_007074.1:g.176453G=

Transcript Alleles

HGVS Amino-acid change
ENST00000272895.12:c.5779-22G= MANE Select ENSP00000272895.7:n.5779-22G=
ENST00000272895.11:c.5779-22G= ENSP00000272895.7:n.5779-22G=
ENST00000389661.4:c.4825-22G= ENSP00000374312.4:n.4825-22G=
NM_015657.3:c.4825-22G= NP_056472.2:n.4825-22G=
NM_173076.2:c.5779-22G= NP_775099.2:n.5779-22G=
NR_103740.1:n.6079-22G=
XM_011510951.1:c.5788-22G= XP_011509253.1:n.5788-22G=
XM_011510952.1:c.5788-22G= XP_011509254.1:n.5788-22G=
XM_011510951.2:c.5788-22G= XP_011509253.1:n.5788-22G=
NM_173076.3:c.5779-22G= MANE Select NP_775099.2:n.5779-22G=
NR_103740.2:n.6277-22G=
NM_015657.4:c.4825-22G= NP_056472.2:n.4825-22G=