Canonical Allele Identifier: CA2243491396
Gene: PAFAH1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.2674118C= , CM000679.2:g.2674118C= GRCh38
NC_000017.10:g.2577412C= , CM000679.1:g.2577412C= GRCh37
NC_000017.9:g.2524162C= NCBI36
NG_009799.1:g.85490C=

Transcript Alleles

HGVS Amino-acid change
ENST00000397195.10:c.730C= MANE Select ENSP00000380378.4:p.Gln244=
ENST00000571495.2:n.1815C=
ENST00000674608.1:c.784C= ENSP00000501976.1:p.Gln262=
ENST00000674717.1:c.535C= ENSP00000501931.1:p.Gln179=
ENST00000675202.1:c.730C= ENSP00000502843.1:p.Gln244=
ENST00000675331.1:c.730C= ENSP00000502031.1:p.Gln244=
ENST00000675390.1:c.730C= ENSP00000501969.1:p.Gln244=
ENST00000675574.1:n.1802C=
ENST00000675621.1:c.730C= ENSP00000502117.1:p.Gln244=
ENST00000675764.1:c.*684C= ENSP00000502242.1:n.*684C=
ENST00000676077.1:c.*48C= ENSP00000502507.1:n.*48C=
ENST00000676098.1:c.730C= ENSP00000502735.1:p.Gln244=
ENST00000676188.1:c.730C= ENSP00000502577.1:p.Gln244=
ENST00000676353.1:c.535C= ENSP00000502737.1:p.Gln179=
ENST00000397193.7:n.538C=
ENST00000397195.9:c.730C= ENSP00000380378.4:p.Gln244=
ENST00000571495.1:n.454C=
ENST00000572915.6:n.676+22C=
ENST00000574468.1:c.226C= ENSP00000460591.1:p.Gln76=
ENST00000574816.5:n.31-2196C=
NM_000430.3:c.730C= NP_000421.1:p.Gln244=
XM_011523901.1:c.784C= XP_011522203.1:p.Gln262=
XM_011523902.1:c.784C= XP_011522204.1:p.Gln262=
XM_011523903.1:c.784C= XP_011522205.1:p.Gln262=
XM_011523904.1:c.*48C= XP_011522206.1:n.*48C=
XM_011523901.2:c.784C= XP_011522203.1:p.Gln262=
XM_011523902.3:c.784C= XP_011522204.1:p.Gln262=
XM_011523903.2:c.784C= XP_011522205.1:p.Gln262=
XM_017024701.1:c.730C= XP_016880190.1:p.Gln244=
XM_017024702.2:c.535C= XP_016880191.1:p.Gln179=
NM_000430.4:c.730C= MANE Select NP_000421.1:p.Gln244=