Canonical Allele Identifier: CA380703220

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57379338C>A (hg19) ; chr11:g.57611865C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611865C>A , CM000673.2:g.57611865C>A	GRCh38
NC_000011.9:g.57379338C>A , CM000673.1:g.57379338C>A	GRCh37
NC_000011.8:g.57135914C>A	NCBI36
NG_009625.1:g.19312C>A , LRG_105:g.19312C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1178C>A MANE Select	ENSP00000278407.4:p.Pro393His
ENST00000528996.2:c.*75C>A	ENSP00000431226.2:n.*75C>A
ENST00000531605.2:c.*954C>A	ENSP00000503752.1:n.*954C>A
ENST00000619430.2:c.974C>A	ENSP00000478572.2:p.Pro325His
ENST00000676670.1:c.1178C>A	ENSP00000504807.1:p.Pro393His
ENST00000676741.1:n.2260C>A
ENST00000677624.1:c.*598C>A	ENSP00000503979.1:n.*598C>A
ENST00000677625.1:c.1124C>A	ENSP00000502857.1:p.Pro375His
ENST00000677856.1:n.1431C>A
ENST00000677915.1:c.*75C>A	ENSP00000503118.1:n.*75C>A
ENST00000678533.1:c.*732C>A	ENSP00000503873.1:n.*732C>A
ENST00000678592.1:c.*118C>A	ENSP00000504424.1:n.*118C>A
ENST00000278407.8:c.1178C>A	ENSP00000278407.4:p.Pro393His
ENST00000340687.10:c.1067C>A	ENSP00000341861.6:p.Pro356His
ENST00000378323.8:c.1193C>A	ENSP00000367574.4:p.Pro398His
ENST00000378324.6:c.1022C>A	ENSP00000367575.2:p.Pro341His
ENST00000403558.1:c.1307C>A	ENSP00000384420.1:p.Pro436His
ENST00000528996.1:c.379C>A	ENSP00000431226.1:n.379C>A
ENST00000530113.1:n.635C>A
ENST00000531133.5:c.679C>A	ENSP00000435431.1:n.679C>A
ENST00000531797.5:c.*203C>A	ENSP00000432554.1:n.*203C>A
ENST00000619430.1:c.349-40C>A	ENSP00000478572.1:n.349-40C>A
NM_000062.2:c.1178C>A , LRG_105t1:c.1178C>A	NP_000053.2:p.Pro393His
NM_001032295.1:c.1178C>A	NP_001027466.1:p.Pro393His
NM_000062.3:c.1178C>A MANE Select	NP_000053.2:p.Pro393His
NM_001032295.2:c.1178C>A	NP_001027466.1:p.Pro393His