Canonical Allele Identifier: CA1618785407
Gene: ABCF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30580433A= , CM000668.2:g.30580433A= GRCh38
NC_000006.11:g.30548210A= , CM000668.1:g.30548210A= GRCh37
NC_000006.10:g.30656189A= NCBI36
NG_047030.1:g.14041A=

Transcript Alleles

HGVS Amino-acid Change
NM_001025091.2:c.592A= MANE Select NP_001020262.1:p.Asn198=
ENST00000326195.13:c.592A= MANE Select ENSP00000313603.8:p.Asn198=
NM_001025091.1:c.592A= NP_001020262.1:p.Asn198=
NM_001090.2:c.592A= NP_001081.1:p.Asn198=
NM_001090.3:c.592A= NP_001081.1:p.Asn198=
ENST00000326195.12:c.592A= ENSP00000313603.8:p.Asn198=
ENST00000376545.7:c.592A= ENSP00000365728.3:p.Asn198=
ENST00000441867.5:c.595A= ENSP00000405512.1:p.Asn199=
ENST00000441867.6:c.595A= ENSP00000405512.2:p.Asn199=
ENST00000468958.1:c.301A= ENSP00000440893.1:p.Asn101=