Canonical Allele Identifier: CA474806727

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381841G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614368G>C , CM000673.2:g.57614368G>C	GRCh38
NC_000011.9:g.57381841G>C , CM000673.1:g.57381841G>C	GRCh37
NC_000011.8:g.57138417G>C	NCBI36
NG_009625.1:g.21815G>C , LRG_105:g.21815G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1290G>C MANE Select	ENSP00000278407.4:p.Leu430=
ENST00000528996.2:c.*187G>C	ENSP00000431226.2:n.*187G>C
ENST00000531605.2:c.*1066G>C	ENSP00000503752.1:n.*1066G>C
ENST00000619430.2:c.1086G>C	ENSP00000478572.2:p.Leu362=
ENST00000676670.1:c.1290G>C	ENSP00000504807.1:p.Leu430=
ENST00000676741.1:n.2372G>C
ENST00000677624.1:c.*710G>C	ENSP00000503979.1:n.*710G>C
ENST00000677625.1:c.1236G>C	ENSP00000502857.1:p.Leu412=
ENST00000677856.1:n.1543G>C
ENST00000677915.1:c.*187G>C	ENSP00000503118.1:n.*187G>C
ENST00000678533.1:c.*844G>C	ENSP00000503873.1:n.*844G>C
ENST00000678592.1:c.*230G>C	ENSP00000504424.1:n.*230G>C
ENST00000278407.8:c.1290G>C	ENSP00000278407.4:p.Leu430=
ENST00000340687.10:c.1179G>C	ENSP00000341861.6:p.Leu393=
ENST00000378323.8:c.1305G>C	ENSP00000367574.4:p.Leu435=
ENST00000378324.6:c.1134G>C	ENSP00000367575.2:p.Leu378=
ENST00000403558.1:c.1419G>C	ENSP00000384420.1:p.Leu473=
ENST00000528996.1:c.491G>C	ENSP00000431226.1:n.491G>C
ENST00000530113.1:n.747G>C
ENST00000531133.5:c.791G>C	ENSP00000435431.1:n.791G>C
ENST00000531797.5:c.*315G>C	ENSP00000432554.1:n.*315G>C
ENST00000619430.1:c.421G>C	ENSP00000478572.1:n.421G>C
NM_000062.2:c.1290G>C , LRG_105t1:c.1290G>C	NP_000053.2:p.Leu430=
NM_001032295.1:c.1290G>C	NP_001027466.1:p.Leu430=
NM_000062.3:c.1290G>C MANE Select	NP_000053.2:p.Leu430=
NM_001032295.2:c.1290G>C	NP_001027466.1:p.Leu430=