Canonical Allele Identifier: CA380698583

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57373500A>C (hg19) ; chr11:g.57606027A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57606027A>C , CM000673.2:g.57606027A>C	GRCh38
NC_000011.9:g.57373500A>C , CM000673.1:g.57373500A>C	GRCh37
NC_000011.8:g.57130076A>C	NCBI36
NG_009625.1:g.13474A>C , LRG_105:g.13474A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.703A>C MANE Select	ENSP00000278407.4:p.Thr235Pro
ENST00000528996.2:c.59-5699A>C	ENSP00000431226.2:n.59-5699A>C
ENST00000531605.2:c.*479A>C	ENSP00000503752.1:n.*479A>C
ENST00000619430.2:c.686-381A>C	ENSP00000478572.2:n.686-381A>C
ENST00000676670.1:c.703A>C	ENSP00000504807.1:p.Thr235Pro
ENST00000676741.1:n.1785A>C
ENST00000677624.1:c.*123A>C	ENSP00000503979.1:n.*123A>C
ENST00000677625.1:c.703A>C	ENSP00000502857.1:p.Thr235Pro
ENST00000677856.1:n.762A>C
ENST00000677915.1:c.685+3858A>C	ENSP00000503118.1:n.685+3858A>C
ENST00000678533.1:c.*257A>C	ENSP00000503873.1:n.*257A>C
ENST00000678592.1:c.703A>C	ENSP00000504424.1:p.Thr235Pro
ENST00000278407.8:c.703A>C	ENSP00000278407.4:p.Thr235Pro
ENST00000340687.10:c.703A>C	ENSP00000341861.6:p.Thr235Pro
ENST00000378323.8:c.718A>C	ENSP00000367574.4:p.Thr240Pro
ENST00000378324.6:c.547A>C	ENSP00000367575.2:p.Thr183Pro
ENST00000403558.1:c.805A>C	ENSP00000384420.1:p.Thr269Pro
ENST00000531133.5:c.204A>C	ENSP00000435431.1:n.204A>C
ENST00000531605.1:n.550A>C
ENST00000531797.5:c.*54+3858A>C	ENSP00000432554.1:n.*54+3858A>C
ENST00000619430.1:c.348+5852A>C	ENSP00000478572.1:n.348+5852A>C
NM_000062.2:c.703A>C , LRG_105t1:c.703A>C	NP_000053.2:p.Thr235Pro
NM_001032295.1:c.703A>C	NP_001027466.1:p.Thr235Pro
NM_000062.3:c.703A>C MANE Select	NP_000053.2:p.Thr235Pro
NM_001032295.2:c.703A>C	NP_001027466.1:p.Thr235Pro