Canonical Allele Identifier: CA380700172

Gene: SERPING1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57606426T>C , CM000673.2:g.57606426T>C	GRCh38
NC_000011.9:g.57373899T>C , CM000673.1:g.57373899T>C	GRCh37
NC_000011.8:g.57130475T>C	NCBI36
NG_009625.1:g.13873T>C , LRG_105:g.13873T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000062.3:c.908T>C MANE Select	NP_000053.2:p.Phe303Ser
ENST00000278407.9:c.908T>C MANE Select	ENSP00000278407.4:p.Phe303Ser
NM_000062.2:c.908T>C , LRG_105t1:c.908T>C	NP_000053.2:p.Phe303Ser
NM_001032295.1:c.908T>C	NP_001027466.1:p.Phe303Ser
NM_001032295.2:c.908T>C	NP_001027466.1:p.Phe303Ser
ENST00000278407.8:c.908T>C	ENSP00000278407.4:p.Phe303Ser
ENST00000340687.10:c.908T>C	ENSP00000341861.6:p.Phe303Ser
ENST00000378323.8:c.923T>C	ENSP00000367574.4:p.Phe308Ser
ENST00000378324.6:c.752T>C	ENSP00000367575.2:p.Phe251Ser
ENST00000403558.1:c.1037T>C	ENSP00000384420.1:p.Phe346Ser
ENST00000528996.1:c.20T>C	ENSP00000431226.1:p.Phe7Ser
ENST00000528996.2:c.59-5300T>C	ENSP00000431226.2:n.59-5300T>C
ENST00000531133.5:c.409T>C	ENSP00000435431.1:n.409T>C
ENST00000531605.2:c.*684T>C	ENSP00000503752.1:n.*684T>C
ENST00000531797.5:c.*54+4257T>C	ENSP00000432554.1:n.*54+4257T>C
ENST00000619430.1:c.349-5479T>C	ENSP00000478572.1:n.349-5479T>C
ENST00000619430.2:c.704T>C	ENSP00000478572.2:p.Phe235Ser
ENST00000676670.1:c.908T>C	ENSP00000504807.1:p.Phe303Ser
ENST00000676741.1:n.1990T>C
ENST00000677624.1:c.*328T>C	ENSP00000503979.1:n.*328T>C
ENST00000677625.1:c.908T>C	ENSP00000502857.1:p.Phe303Ser
ENST00000677856.1:n.1161T>C
ENST00000677915.1:c.685+4257T>C	ENSP00000503118.1:n.685+4257T>C
ENST00000678533.1:c.*462T>C	ENSP00000503873.1:n.*462T>C
ENST00000678592.1:c.908T>C	ENSP00000504424.1:p.Phe303Ser