Canonical Allele Identifier: CA380703213

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57379337C>A (hg19) ; chr11:g.57611864C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611864C>A , CM000673.2:g.57611864C>A	GRCh38
NC_000011.9:g.57379337C>A , CM000673.1:g.57379337C>A	GRCh37
NC_000011.8:g.57135913C>A	NCBI36
NG_009625.1:g.19311C>A , LRG_105:g.19311C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1177C>A MANE Select	ENSP00000278407.4:p.Pro393Thr
ENST00000528996.2:c.*74C>A	ENSP00000431226.2:n.*74C>A
ENST00000531605.2:c.*953C>A	ENSP00000503752.1:n.*953C>A
ENST00000619430.2:c.973C>A	ENSP00000478572.2:p.Pro325Thr
ENST00000676670.1:c.1177C>A	ENSP00000504807.1:p.Pro393Thr
ENST00000676741.1:n.2259C>A
ENST00000677624.1:c.*597C>A	ENSP00000503979.1:n.*597C>A
ENST00000677625.1:c.1123C>A	ENSP00000502857.1:p.Pro375Thr
ENST00000677856.1:n.1430C>A
ENST00000677915.1:c.*74C>A	ENSP00000503118.1:n.*74C>A
ENST00000678533.1:c.*731C>A	ENSP00000503873.1:n.*731C>A
ENST00000678592.1:c.*117C>A	ENSP00000504424.1:n.*117C>A
ENST00000278407.8:c.1177C>A	ENSP00000278407.4:p.Pro393Thr
ENST00000340687.10:c.1066C>A	ENSP00000341861.6:p.Pro356Thr
ENST00000378323.8:c.1192C>A	ENSP00000367574.4:p.Pro398Thr
ENST00000378324.6:c.1021C>A	ENSP00000367575.2:p.Pro341Thr
ENST00000403558.1:c.1306C>A	ENSP00000384420.1:p.Pro436Thr
ENST00000528996.1:c.378C>A	ENSP00000431226.1:n.378C>A
ENST00000530113.1:n.634C>A
ENST00000531133.5:c.678C>A	ENSP00000435431.1:n.678C>A
ENST00000531797.5:c.*202C>A	ENSP00000432554.1:n.*202C>A
ENST00000619430.1:c.349-41C>A	ENSP00000478572.1:n.349-41C>A
NM_000062.2:c.1177C>A , LRG_105t1:c.1177C>A	NP_000053.2:p.Pro393Thr
NM_001032295.1:c.1177C>A	NP_001027466.1:p.Pro393Thr
NM_000062.3:c.1177C>A MANE Select	NP_000053.2:p.Pro393Thr
NM_001032295.2:c.1177C>A	NP_001027466.1:p.Pro393Thr