Canonical Allele Identifier: CA2635351502

Gene: PAFAH1B1

Linked Data

• gnomAD v4: 17-2676392-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.2676392_2676393insG , CM000679.2:g.2676392_2676393insG	GRCh38
NC_000017.10:g.2579686_2579687insG , CM000679.1:g.2579686_2579687insG	GRCh37
NC_000017.9:g.2526436_2526437insG	NCBI36
NG_009799.1:g.87764_87765insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397195.10:c.901-113_901-112insG MANE Select	ENSP00000380378.4:n.901-113_901-112insG
ENST00000571495.2:n.1986-113_1986-112insG
ENST00000674608.1:c.955-113_955-112insG	ENSP00000501976.1:n.955-113_955-112insG
ENST00000674717.1:c.706-113_706-112insG	ENSP00000501931.1:n.706-113_706-112insG
ENST00000675084.1:n.42_43insG
ENST00000675202.1:c.901-113_901-112insG	ENSP00000502843.1:n.901-113_901-112insG
ENST00000675331.1:c.901-113_901-112insG	ENSP00000502031.1:n.901-113_901-112insG
ENST00000675385.1:n.402_403insG
ENST00000675390.1:c.901-113_901-112insG	ENSP00000501969.1:n.901-113_901-112insG
ENST00000675574.1:n.3843_3844insG
ENST00000675621.1:c.901-113_901-112insG	ENSP00000502117.1:n.901-113_901-112insG
ENST00000675764.1:c.*855-113_*855-112insG	ENSP00000502242.1:n.*855-113_*855-112insG
ENST00000676077.1:c.*219-113_*219-112insG	ENSP00000502507.1:n.*219-113_*219-112insG
ENST00000676098.1:c.901-113_901-112insG	ENSP00000502735.1:n.901-113_901-112insG
ENST00000676188.1:c.901-113_901-112insG	ENSP00000502577.1:n.901-113_901-112insG
ENST00000676353.1:c.706-113_706-112insG	ENSP00000502737.1:n.706-113_706-112insG
ENST00000397193.7:n.709-113_709-112insG
ENST00000397195.9:c.901-113_901-112insG	ENSP00000380378.4:n.901-113_901-112insG
ENST00000571495.1:n.625-113_625-112insG
ENST00000572915.6:n.676+2296_676+2297insG
ENST00000574468.1:c.396+2104_396+2105insG	ENSP00000460591.1:n.396+2104_396+2105insG
ENST00000574816.5:n.109_110insG
NM_000430.3:c.901-113_901-112insG	NP_000421.1:n.901-113_901-112insG
XM_011523901.1:c.955-113_955-112insG	XP_011522203.1:n.955-113_955-112insG
XM_011523902.1:c.955-113_955-112insG	XP_011522204.1:n.955-113_955-112insG
XM_011523903.1:c.955-113_955-112insG	XP_011522205.1:n.955-113_955-112insG
XM_011523901.2:c.955-113_955-112insG	XP_011522203.1:n.955-113_955-112insG
XM_011523902.3:c.955-113_955-112insG	XP_011522204.1:n.955-113_955-112insG
XM_011523903.2:c.955-113_955-112insG	XP_011522205.1:n.955-113_955-112insG
XM_017024701.1:c.901-113_901-112insG	XP_016880190.1:n.901-113_901-112insG
XM_017024702.2:c.706-113_706-112insG	XP_016880191.1:n.706-113_706-112insG
NM_000430.4:c.901-113_901-112insG MANE Select	NP_000421.1:n.901-113_901-112insG