Canonical Allele Identifier: CA380690739

Gene: SERPING1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614472C>G , CM000673.2:g.57614472C>G	GRCh38
NC_000011.9:g.57381945C>G , CM000673.1:g.57381945C>G	GRCh37
NC_000011.8:g.57138521C>G	NCBI36
NG_009625.1:g.21919C>G , LRG_105:g.21919C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000062.3:c.1394C>G MANE Select	NP_000053.2:p.Ala465Gly
ENST00000278407.9:c.1394C>G MANE Select	ENSP00000278407.4:p.Ala465Gly
NM_000062.2:c.1394C>G , LRG_105t1:c.1394C>G	NP_000053.2:p.Ala465Gly
NM_001032295.1:c.1394C>G	NP_001027466.1:p.Ala465Gly
NM_001032295.2:c.1394C>G	NP_001027466.1:p.Ala465Gly
ENST00000278407.8:c.1394C>G	ENSP00000278407.4:p.Ala465Gly
ENST00000340687.10:c.1283C>G	ENSP00000341861.6:p.Ala428Gly
ENST00000378323.8:c.1409C>G	ENSP00000367574.4:p.Ala470Gly
ENST00000378324.6:c.1238C>G	ENSP00000367575.2:p.Ala413Gly
ENST00000403558.1:c.1523C>G	ENSP00000384420.1:p.Ala508Gly
ENST00000528996.1:c.595C>G	ENSP00000431226.1:n.595C>G
ENST00000528996.2:c.*291C>G	ENSP00000431226.2:n.*291C>G
ENST00000530113.1:n.851C>G
ENST00000531133.5:c.895C>G	ENSP00000435431.1:n.895C>G
ENST00000531605.2:c.*1170C>G	ENSP00000503752.1:n.*1170C>G
ENST00000531797.5:c.*419C>G	ENSP00000432554.1:n.*419C>G
ENST00000619430.1:c.525C>G	ENSP00000478572.1:n.525C>G
ENST00000619430.2:c.1190C>G	ENSP00000478572.2:p.Ala397Gly
ENST00000676670.1:c.1394C>G	ENSP00000504807.1:p.Ala465Gly
ENST00000676741.1:n.2476C>G
ENST00000677624.1:c.*814C>G	ENSP00000503979.1:n.*814C>G
ENST00000677625.1:c.1340C>G	ENSP00000502857.1:p.Ala447Gly
ENST00000677856.1:n.1647C>G
ENST00000677915.1:c.*291C>G	ENSP00000503118.1:n.*291C>G
ENST00000678533.1:c.*948C>G	ENSP00000503873.1:n.*948C>G
ENST00000678592.1:c.*334C>G	ENSP00000504424.1:n.*334C>G