Canonical Allele Identifier: CA397642263

Gene: PAFAH1B1

Linked Data

• MyVariant Identifiers: chr17:g.2579864G>C (hg19) ; chr17:g.2676570G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.2676570G>C , CM000679.2:g.2676570G>C	GRCh38
NC_000017.10:g.2579864G>C , CM000679.1:g.2579864G>C	GRCh37
NC_000017.9:g.2526614G>C	NCBI36
NG_009799.1:g.87942G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397195.10:c.966G>C MANE Select	ENSP00000380378.4:p.Met322Ile
ENST00000571495.2:n.2051G>C
ENST00000674608.1:c.1020G>C	ENSP00000501976.1:p.Met340Ile
ENST00000674717.1:c.771G>C	ENSP00000501931.1:p.Met257Ile
ENST00000675084.1:n.220G>C
ENST00000675202.1:c.966G>C	ENSP00000502843.1:p.Met322Ile
ENST00000675331.1:c.966G>C	ENSP00000502031.1:p.Met322Ile
ENST00000675385.1:n.580G>C
ENST00000675390.1:c.966G>C	ENSP00000501969.1:p.Met322Ile
ENST00000675574.1:n.4021G>C
ENST00000675621.1:c.966G>C	ENSP00000502117.1:p.Met322Ile
ENST00000675764.1:c.*920G>C	ENSP00000502242.1:n.*920G>C
ENST00000676077.1:c.*284G>C	ENSP00000502507.1:n.*284G>C
ENST00000676098.1:c.966G>C	ENSP00000502735.1:p.Met322Ile
ENST00000676188.1:c.966G>C	ENSP00000502577.1:p.Met322Ile
ENST00000676353.1:c.771G>C	ENSP00000502737.1:p.Met257Ile
ENST00000397193.7:n.774G>C
ENST00000397195.9:c.966G>C	ENSP00000380378.4:p.Met322Ile
ENST00000571495.1:n.690G>C
ENST00000572915.6:n.676+2474G>C
ENST00000574468.1:c.396+2282G>C	ENSP00000460591.1:n.396+2282G>C
ENST00000574816.5:n.287G>C
NM_000430.3:c.966G>C	NP_000421.1:p.Met322Ile
XM_011523901.1:c.1020G>C	XP_011522203.1:p.Met340Ile
XM_011523902.1:c.1020G>C	XP_011522204.1:p.Met340Ile
XM_011523903.1:c.1020G>C	XP_011522205.1:p.Met340Ile
XM_011523901.2:c.1020G>C	XP_011522203.1:p.Met340Ile
XM_011523902.3:c.1020G>C	XP_011522204.1:p.Met340Ile
XM_011523903.2:c.1020G>C	XP_011522205.1:p.Met340Ile
XM_017024701.1:c.966G>C	XP_016880190.1:p.Met322Ile
XM_017024702.2:c.771G>C	XP_016880191.1:p.Met257Ile
NM_000430.4:c.966G>C MANE Select	NP_000421.1:p.Met322Ile