Canonical Allele Identifier: CA8283294

Gene: PAFAH1B1

Linked Data

• dbSNP Id: rs756692080
• ExAC: 17:2579914 A / ATCTTACCATT
• MyVariant Identifiers: chr17:g.2579914_2579915insTCTTACCATT (hg19) ; chr17:g.2676620_2676621insTCTTACCATT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.2676625_2676634dup , CM000679.2:g.2676625_2676634dup	GRCh38
NC_000017.10:g.2579919_2579928dup , CM000679.1:g.2579919_2579928dup	GRCh37
NC_000017.9:g.2526669_2526678dup	NCBI36
NG_009799.1:g.87997_88006dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000397195.10:c.1002+19_1002+28dup MANE Select	ENSP00000380378.4:n.1002+19_1002+28dup
ENST00000571495.2:n.2087+19_2087+28dup
ENST00000674608.1:c.1056+19_1056+28dup	ENSP00000501976.1:n.1056+19_1056+28dup
ENST00000674717.1:c.807+19_807+28dup	ENSP00000501931.1:n.807+19_807+28dup
ENST00000675084.1:n.256+19_256+28dup
ENST00000675202.1:c.1002+19_1002+28dup	ENSP00000502843.1:n.1002+19_1002+28dup
ENST00000675331.1:c.1002+19_1002+28dup	ENSP00000502031.1:n.1002+19_1002+28dup
ENST00000675385.1:n.616+19_616+28dup
ENST00000675390.1:c.1002+19_1002+28dup	ENSP00000501969.1:n.1002+19_1002+28dup
ENST00000675574.1:n.4057+19_4057+28dup
ENST00000675621.1:c.1002+19_1002+28dup	ENSP00000502117.1:n.1002+19_1002+28dup
ENST00000675764.1:c.*956+19_*956+28dup	ENSP00000502242.1:n.*956+19_*956+28dup
ENST00000676077.1:c.*320+19_*320+28dup	ENSP00000502507.1:n.*320+19_*320+28dup
ENST00000676098.1:c.1002+19_1002+28dup	ENSP00000502735.1:n.1002+19_1002+28dup
ENST00000676188.1:c.1002+19_1002+28dup	ENSP00000502577.1:n.1002+19_1002+28dup
ENST00000676353.1:c.807+19_807+28dup	ENSP00000502737.1:n.807+19_807+28dup
ENST00000397193.7:n.810+19_810+28dup
ENST00000397195.9:c.1002+19_1002+28dup	ENSP00000380378.4:n.1002+19_1002+28dup
ENST00000571495.1:n.726+19_726+28dup
ENST00000572915.6:n.676+2529_676+2538dup
ENST00000574468.1:c.396+2337_396+2346dup	ENSP00000460591.1:n.396+2337_396+2346dup
ENST00000574816.5:n.323+19_323+28dup
NM_000430.3:c.1002+19_1002+28dup	NP_000421.1:n.1002+19_1002+28dup
XM_011523901.1:c.1056+19_1056+28dup	XP_011522203.1:n.1056+19_1056+28dup
XM_011523902.1:c.1056+19_1056+28dup	XP_011522204.1:n.1056+19_1056+28dup
XM_011523903.1:c.1056+19_1056+28dup	XP_011522205.1:n.1056+19_1056+28dup
XM_011523901.2:c.1056+19_1056+28dup	XP_011522203.1:n.1056+19_1056+28dup
XM_011523902.3:c.1056+19_1056+28dup	XP_011522204.1:n.1056+19_1056+28dup
XM_011523903.2:c.1056+19_1056+28dup	XP_011522205.1:n.1056+19_1056+28dup
XM_017024701.1:c.1002+19_1002+28dup	XP_016880190.1:n.1002+19_1002+28dup
XM_017024702.2:c.807+19_807+28dup	XP_016880191.1:n.807+19_807+28dup
NM_000430.4:c.1002+19_1002+28dup MANE Select	NP_000421.1:n.1002+19_1002+28dup