Canonical Allele Identifier: CA1327196970
Gene: ABCA12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.215064105A= , CM000664.2:g.215064105A= GRCh38
NC_000002.11:g.215928828A= , CM000664.1:g.215928828A= GRCh37
NC_000002.10:g.215637073A= NCBI36
NG_007074.1:g.79324T=

Transcript Alleles

HGVS Amino-acid change
ENST00000272895.12:c.278T= MANE Select ENSP00000272895.7:p.Leu93=
ENST00000272895.11:c.278T= ENSP00000272895.7:p.Leu93=
NM_173076.2:c.278T= NP_775099.2:p.Leu93=
NR_103740.1:n.498T=
XM_011510951.1:c.278T= XP_011509253.1:p.Leu93=
XM_011510952.1:c.278T= XP_011509254.1:p.Leu93=
XM_011510951.2:c.278T= XP_011509253.1:p.Leu93=
NM_173076.3:c.278T= MANE Select NP_775099.2:p.Leu93=
NR_103740.2:n.696T=