Canonical Allele Identifier: CA380690667

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381912T>C (hg19) ; chr11:g.57614439T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614439T>C , CM000673.2:g.57614439T>C	GRCh38
NC_000011.9:g.57381912T>C , CM000673.1:g.57381912T>C	GRCh37
NC_000011.8:g.57138488T>C	NCBI36
NG_009625.1:g.21886T>C , LRG_105:g.21886T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1361T>C MANE Select	ENSP00000278407.4:p.Val454Ala
ENST00000528996.2:c.*258T>C	ENSP00000431226.2:n.*258T>C
ENST00000531605.2:c.*1137T>C	ENSP00000503752.1:n.*1137T>C
ENST00000619430.2:c.1157T>C	ENSP00000478572.2:p.Val386Ala
ENST00000676670.1:c.1361T>C	ENSP00000504807.1:p.Val454Ala
ENST00000676741.1:n.2443T>C
ENST00000677624.1:c.*781T>C	ENSP00000503979.1:n.*781T>C
ENST00000677625.1:c.1307T>C	ENSP00000502857.1:p.Val436Ala
ENST00000677856.1:n.1614T>C
ENST00000677915.1:c.*258T>C	ENSP00000503118.1:n.*258T>C
ENST00000678533.1:c.*915T>C	ENSP00000503873.1:n.*915T>C
ENST00000678592.1:c.*301T>C	ENSP00000504424.1:n.*301T>C
ENST00000278407.8:c.1361T>C	ENSP00000278407.4:p.Val454Ala
ENST00000340687.10:c.1250T>C	ENSP00000341861.6:p.Val417Ala
ENST00000378323.8:c.1376T>C	ENSP00000367574.4:p.Val459Ala
ENST00000378324.6:c.1205T>C	ENSP00000367575.2:p.Val402Ala
ENST00000403558.1:c.1490T>C	ENSP00000384420.1:p.Val497Ala
ENST00000528996.1:c.562T>C	ENSP00000431226.1:n.562T>C
ENST00000530113.1:n.818T>C
ENST00000531133.5:c.862T>C	ENSP00000435431.1:n.862T>C
ENST00000531797.5:c.*386T>C	ENSP00000432554.1:n.*386T>C
ENST00000619430.1:c.492T>C	ENSP00000478572.1:n.492T>C
NM_000062.2:c.1361T>C , LRG_105t1:c.1361T>C	NP_000053.2:p.Val454Ala
NM_001032295.1:c.1361T>C	NP_001027466.1:p.Val454Ala
NM_000062.3:c.1361T>C MANE Select	NP_000053.2:p.Val454Ala
NM_001032295.2:c.1361T>C	NP_001027466.1:p.Val454Ala