Canonical Allele Identifier: CA371078745

Gene: PLAT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.42182000G>A , CM000670.2:g.42182000G>A	GRCh38
NC_000008.10:g.42039518G>A , CM000670.1:g.42039518G>A	GRCh37
NC_000008.9:g.42158675G>A	NCBI36
NG_023264.1:g.30677C>T , LRG_570:g.30677C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000930.5:c.826C>T MANE Select	NP_000921.1:p.Pro276Ser
ENST00000220809.9:c.826C>T MANE Select	ENSP00000220809.4:p.Pro276Ser
NM_000930.3:c.826C>T , LRG_570t1:c.826C>T	NP_000921.1:p.Pro276Ser
NM_000930.4:c.826C>T	NP_000921.1:p.Pro276Ser
NM_001319189.1:c.559C>T	NP_001306118.1:p.Pro187Ser
NM_001319189.2:c.559C>T	NP_001306118.1:p.Pro187Ser
NM_033011.2:c.688C>T	NP_127509.1:p.Pro230Ser
NM_033011.3:c.688C>T	NP_127509.1:p.Pro230Ser
NM_033011.4:c.688C>T	NP_127509.1:p.Pro230Ser
ENST00000220809.8:c.826C>T	ENSP00000220809.4:p.Pro276Ser
ENST00000352041.7:c.688C>T	ENSP00000270188.6:p.Pro230Ser
ENST00000429089.6:c.826C>T	ENSP00000392045.2:p.Pro276Ser
ENST00000429710.6:c.448C>T	ENSP00000407861.2:p.Pro150Ser
ENST00000519510.5:c.637C>T	ENSP00000428886.1:p.Pro213Ser
ENST00000521042.1:c.272C>T
ENST00000524009.5:c.559C>T	ENSP00000429401.1:p.Pro187Ser
ENST00000677722.1:n.1764C>T
ENST00000678083.1:c.826C>T	ENSP00000504824.1:p.Pro276Ser
ENST00000678676.1:c.*185C>T	ENSP00000502858.1:n.*185C>T
ENST00000679151.1:c.826C>T	ENSP00000504311.1:p.Pro276Ser
ENST00000679300.1:c.826C>T	ENSP00000503050.1:p.Pro276Ser