Canonical Allele Identifier: CA380690424

Gene: SERPING1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614387C>T , CM000673.2:g.57614387C>T	GRCh38
NC_000011.9:g.57381860C>T , CM000673.1:g.57381860C>T	GRCh37
NC_000011.8:g.57138436C>T	NCBI36
NG_009625.1:g.21834C>T , LRG_105:g.21834C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000062.3:c.1309C>T MANE Select	NP_000053.2:p.Gln437Ter
ENST00000278407.9:c.1309C>T MANE Select	ENSP00000278407.4:p.Gln437Ter
NM_000062.2:c.1309C>T , LRG_105t1:c.1309C>T	NP_000053.2:p.Gln437Ter
NM_001032295.1:c.1309C>T	NP_001027466.1:p.Gln437Ter
NM_001032295.2:c.1309C>T	NP_001027466.1:p.Gln437Ter
ENST00000278407.8:c.1309C>T	ENSP00000278407.4:p.Gln437Ter
ENST00000340687.10:c.1198C>T	ENSP00000341861.6:p.Gln400Ter
ENST00000378323.8:c.1324C>T	ENSP00000367574.4:p.Gln442Ter
ENST00000378324.6:c.1153C>T	ENSP00000367575.2:p.Gln385Ter
ENST00000403558.1:c.1438C>T	ENSP00000384420.1:p.Gln480Ter
ENST00000528996.1:c.510C>T	ENSP00000431226.1:n.510C>T
ENST00000528996.2:c.*206C>T	ENSP00000431226.2:n.*206C>T
ENST00000530113.1:n.766C>T
ENST00000531133.5:c.810C>T	ENSP00000435431.1:n.810C>T
ENST00000531605.2:c.*1085C>T	ENSP00000503752.1:n.*1085C>T
ENST00000531797.5:c.*334C>T	ENSP00000432554.1:n.*334C>T
ENST00000619430.1:c.440C>T	ENSP00000478572.1:n.440C>T
ENST00000619430.2:c.1105C>T	ENSP00000478572.2:p.Gln369Ter
ENST00000676670.1:c.1309C>T	ENSP00000504807.1:p.Gln437Ter
ENST00000676741.1:n.2391C>T
ENST00000677624.1:c.*729C>T	ENSP00000503979.1:n.*729C>T
ENST00000677625.1:c.1255C>T	ENSP00000502857.1:p.Gln419Ter
ENST00000677856.1:n.1562C>T
ENST00000677915.1:c.*206C>T	ENSP00000503118.1:n.*206C>T
ENST00000678533.1:c.*863C>T	ENSP00000503873.1:n.*863C>T
ENST00000678592.1:c.*249C>T	ENSP00000504424.1:n.*249C>T