Canonical Allele Identifier: CA397642311
Gene: PAFAH1B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.2676590T>A , CM000679.2:g.2676590T>A GRCh38
NC_000017.10:g.2579884T>A , CM000679.1:g.2579884T>A GRCh37
NC_000017.9:g.2526634T>A NCBI36
NG_009799.1:g.87962T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000397195.10:c.986T>A MANE Select ENSP00000380378.4:p.Met329Lys
ENST00000571495.2:n.2071T>A
ENST00000674608.1:c.1040T>A ENSP00000501976.1:p.Met347Lys
ENST00000674717.1:c.791T>A ENSP00000501931.1:p.Met264Lys
ENST00000675084.1:n.240T>A
ENST00000675202.1:c.986T>A ENSP00000502843.1:p.Met329Lys
ENST00000675331.1:c.986T>A ENSP00000502031.1:p.Met329Lys
ENST00000675385.1:n.600T>A
ENST00000675390.1:c.986T>A ENSP00000501969.1:p.Met329Lys
ENST00000675574.1:n.4041T>A
ENST00000675621.1:c.986T>A ENSP00000502117.1:p.Met329Lys
ENST00000675764.1:c.*940T>A ENSP00000502242.1:n.*940T>A
ENST00000676077.1:c.*304T>A ENSP00000502507.1:n.*304T>A
ENST00000676098.1:c.986T>A ENSP00000502735.1:p.Met329Lys
ENST00000676188.1:c.986T>A ENSP00000502577.1:p.Met329Lys
ENST00000676353.1:c.791T>A ENSP00000502737.1:p.Met264Lys
ENST00000397193.7:n.794T>A
ENST00000397195.9:c.986T>A ENSP00000380378.4:p.Met329Lys
ENST00000571495.1:n.710T>A
ENST00000572915.6:n.676+2494T>A
ENST00000574468.1:c.396+2302T>A ENSP00000460591.1:n.396+2302T>A
ENST00000574816.5:n.307T>A
NM_000430.3:c.986T>A NP_000421.1:p.Met329Lys
XM_011523901.1:c.1040T>A XP_011522203.1:p.Met347Lys
XM_011523902.1:c.1040T>A XP_011522204.1:p.Met347Lys
XM_011523903.1:c.1040T>A XP_011522205.1:p.Met347Lys
XM_011523901.2:c.1040T>A XP_011522203.1:p.Met347Lys
XM_011523902.3:c.1040T>A XP_011522204.1:p.Met347Lys
XM_011523903.2:c.1040T>A XP_011522205.1:p.Met347Lys
XM_017024701.1:c.986T>A XP_016880190.1:p.Met329Lys
XM_017024702.2:c.791T>A XP_016880191.1:p.Met264Lys
NM_000430.4:c.986T>A MANE Select NP_000421.1:p.Met329Lys