Canonical Allele Identifier: CA380699227

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57373591G>C (hg19) ; chr11:g.57606118G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57606118G>C , CM000673.2:g.57606118G>C	GRCh38
NC_000011.9:g.57373591G>C , CM000673.1:g.57373591G>C	GRCh37
NC_000011.8:g.57130167G>C	NCBI36
NG_009625.1:g.13565G>C , LRG_105:g.13565G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.794G>C MANE Select	ENSP00000278407.4:p.Trp265Ser
ENST00000528996.2:c.59-5608G>C	ENSP00000431226.2:n.59-5608G>C
ENST00000531605.2:c.*570G>C	ENSP00000503752.1:n.*570G>C
ENST00000619430.2:c.686-290G>C	ENSP00000478572.2:n.686-290G>C
ENST00000676670.1:c.794G>C	ENSP00000504807.1:p.Trp265Ser
ENST00000676741.1:n.1876G>C
ENST00000677624.1:c.*214G>C	ENSP00000503979.1:n.*214G>C
ENST00000677625.1:c.794G>C	ENSP00000502857.1:p.Trp265Ser
ENST00000677856.1:n.853G>C
ENST00000677915.1:c.685+3949G>C	ENSP00000503118.1:n.685+3949G>C
ENST00000678533.1:c.*348G>C	ENSP00000503873.1:n.*348G>C
ENST00000678592.1:c.794G>C	ENSP00000504424.1:p.Trp265Ser
ENST00000278407.8:c.794G>C	ENSP00000278407.4:p.Trp265Ser
ENST00000340687.10:c.794G>C	ENSP00000341861.6:p.Trp265Ser
ENST00000378323.8:c.809G>C	ENSP00000367574.4:p.Trp270Ser
ENST00000378324.6:c.638G>C	ENSP00000367575.2:p.Trp213Ser
ENST00000403558.1:c.896G>C	ENSP00000384420.1:p.Trp299Ser
ENST00000531133.5:c.295G>C	ENSP00000435431.1:n.295G>C
ENST00000531797.5:c.*54+3949G>C	ENSP00000432554.1:n.*54+3949G>C
ENST00000619430.1:c.349-5787G>C	ENSP00000478572.1:n.349-5787G>C
NM_000062.2:c.794G>C , LRG_105t1:c.794G>C	NP_000053.2:p.Trp265Ser
NM_001032295.1:c.794G>C	NP_001027466.1:p.Trp265Ser
NM_000062.3:c.794G>C MANE Select	NP_000053.2:p.Trp265Ser
NM_001032295.2:c.794G>C	NP_001027466.1:p.Trp265Ser