Canonical Allele Identifier: CA380702518

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57379233T>C (hg19) ; chr11:g.57611760T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611760T>C , CM000673.2:g.57611760T>C	GRCh38
NC_000011.9:g.57379233T>C , CM000673.1:g.57379233T>C	GRCh37
NC_000011.8:g.57135809T>C	NCBI36
NG_009625.1:g.19207T>C , LRG_105:g.19207T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1073T>C MANE Select	ENSP00000278407.4:p.Leu358Pro
ENST00000528996.2:c.93T>C	ENSP00000431226.2:p.Pro31=
ENST00000531605.2:c.*849T>C	ENSP00000503752.1:n.*849T>C
ENST00000619430.2:c.869T>C	ENSP00000478572.2:p.Leu290Pro
ENST00000676670.1:c.1073T>C	ENSP00000504807.1:p.Leu358Pro
ENST00000676741.1:n.2155T>C
ENST00000677624.1:c.*493T>C	ENSP00000503979.1:n.*493T>C
ENST00000677625.1:c.1030-11T>C	ENSP00000502857.1:n.1030-11T>C
ENST00000677856.1:n.1326T>C
ENST00000677915.1:c.729T>C	ENSP00000503118.1:p.Pro243=
ENST00000678533.1:c.*627T>C	ENSP00000503873.1:n.*627T>C
ENST00000678592.1:c.*13T>C	ENSP00000504424.1:n.*13T>C
ENST00000278407.8:c.1073T>C	ENSP00000278407.4:p.Leu358Pro
ENST00000340687.10:c.1030-68T>C	ENSP00000341861.6:n.1030-68T>C
ENST00000378323.8:c.1088T>C	ENSP00000367574.4:p.Leu363Pro
ENST00000378324.6:c.917T>C	ENSP00000367575.2:p.Leu306Pro
ENST00000403558.1:c.1202T>C	ENSP00000384420.1:p.Leu401Pro
ENST00000528996.1:c.274T>C	ENSP00000431226.1:n.274T>C
ENST00000530113.1:n.530T>C
ENST00000531133.5:c.574T>C	ENSP00000435431.1:n.574T>C
ENST00000531797.5:c.*98T>C	ENSP00000432554.1:n.*98T>C
ENST00000619430.1:c.349-145T>C	ENSP00000478572.1:n.349-145T>C
NM_000062.2:c.1073T>C , LRG_105t1:c.1073T>C	NP_000053.2:p.Leu358Pro
NM_001032295.1:c.1073T>C	NP_001027466.1:p.Leu358Pro
NM_000062.3:c.1073T>C MANE Select	NP_000053.2:p.Leu358Pro
NM_001032295.2:c.1073T>C	NP_001027466.1:p.Leu358Pro