Canonical Allele Identifier: CA1327177584
Community Standard Title: NM_173076.3(ABCA12):c.1300C= (p.Arg434=)
Gene: ABCA12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.215019784G= , CM000664.2:g.215019784G= GRCh38
NC_000002.11:g.215884508G= , CM000664.1:g.215884508G= GRCh37
NC_000002.10:g.215592753G= NCBI36
NG_007074.1:g.123644C=

Transcript Alleles

HGVS Amino-acid Change
NM_173076.3:c.1300C= MANE Select NP_775099.2:p.Arg434=
ENST00000272895.12:c.1300C= MANE Select ENSP00000272895.7:p.Arg434=
NM_015657.3:c.346C= NP_056472.2:p.Arg116=
NM_015657.4:c.346C= NP_056472.2:p.Arg116=
NM_173076.2:c.1300C= NP_775099.2:p.Arg434=
NR_103740.1:n.1544C=
NR_103740.2:n.1742C=
ENST00000272895.11:c.1300C= ENSP00000272895.7:p.Arg434=
ENST00000389661.4:c.346C= ENSP00000374312.4:p.Arg116=
XM_011510951.1:c.1300C= XP_011509253.1:p.Arg434=
XM_011510951.2:c.1300C= XP_011509253.1:p.Arg434=
XM_011510952.1:c.1300C= XP_011509254.1:p.Arg434=