Canonical Allele Identifier: CA727483564

Gene: PAFAH1B1

Linked Data

• dbSNP Id: rs1307839900
• MyVariant Identifiers: chr17:g.2579641_2579642insGA (hg19) ; chr17:g.2676347_2676348insGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.2676347_2676348insGA , CM000679.2:g.2676347_2676348insGA	GRCh38
NC_000017.10:g.2579641_2579642insGA , CM000679.1:g.2579641_2579642insGA	GRCh37
NC_000017.9:g.2526391_2526392insGA	NCBI36
NG_009799.1:g.87719_87720insGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397195.10:c.901-158_901-157insGA MANE Select	ENSP00000380378.4:n.901-158_901-157insGA
ENST00000571495.2:n.1986-158_1986-157insGA
ENST00000674608.1:c.955-158_955-157insGA	ENSP00000501976.1:n.955-158_955-157insGA
ENST00000674717.1:c.706-158_706-157insGA	ENSP00000501931.1:n.706-158_706-157insGA
ENST00000675202.1:c.901-158_901-157insGA	ENSP00000502843.1:n.901-158_901-157insGA
ENST00000675331.1:c.901-158_901-157insGA	ENSP00000502031.1:n.901-158_901-157insGA
ENST00000675385.1:n.357_358insGA
ENST00000675390.1:c.901-158_901-157insGA	ENSP00000501969.1:n.901-158_901-157insGA
ENST00000675574.1:n.3798_3799insGA
ENST00000675621.1:c.901-158_901-157insGA	ENSP00000502117.1:n.901-158_901-157insGA
ENST00000675764.1:c.*855-158_*855-157insGA	ENSP00000502242.1:n.*855-158_*855-157insGA
ENST00000676077.1:c.*219-158_*219-157insGA	ENSP00000502507.1:n.*219-158_*219-157insGA
ENST00000676098.1:c.901-158_901-157insGA	ENSP00000502735.1:n.901-158_901-157insGA
ENST00000676188.1:c.901-158_901-157insGA	ENSP00000502577.1:n.901-158_901-157insGA
ENST00000676353.1:c.706-158_706-157insGA	ENSP00000502737.1:n.706-158_706-157insGA
ENST00000397193.7:n.709-158_709-157insGA
ENST00000397195.9:c.901-158_901-157insGA	ENSP00000380378.4:n.901-158_901-157insGA
ENST00000571495.1:n.625-158_625-157insGA
ENST00000572915.6:n.676+2251_676+2252insGA
ENST00000574468.1:c.396+2059_396+2060insGA	ENSP00000460591.1:n.396+2059_396+2060insGA
ENST00000574816.5:n.64_65insGA
NM_000430.3:c.901-158_901-157insGA	NP_000421.1:n.901-158_901-157insGA
XM_011523901.1:c.955-158_955-157insGA	XP_011522203.1:n.955-158_955-157insGA
XM_011523902.1:c.955-158_955-157insGA	XP_011522204.1:n.955-158_955-157insGA
XM_011523903.1:c.955-158_955-157insGA	XP_011522205.1:n.955-158_955-157insGA
XM_011523901.2:c.955-158_955-157insGA	XP_011522203.1:n.955-158_955-157insGA
XM_011523902.3:c.955-158_955-157insGA	XP_011522204.1:n.955-158_955-157insGA
XM_011523903.2:c.955-158_955-157insGA	XP_011522205.1:n.955-158_955-157insGA
XM_017024701.1:c.901-158_901-157insGA	XP_016880190.1:n.901-158_901-157insGA
XM_017024702.2:c.706-158_706-157insGA	XP_016880191.1:n.706-158_706-157insGA
NM_000430.4:c.901-158_901-157insGA MANE Select	NP_000421.1:n.901-158_901-157insGA