Canonical Allele Identifier: CA380702546

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57379238C>G (hg19) ; chr11:g.57611765C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611765C>G , CM000673.2:g.57611765C>G	GRCh38
NC_000011.9:g.57379238C>G , CM000673.1:g.57379238C>G	GRCh37
NC_000011.8:g.57135814C>G	NCBI36
NG_009625.1:g.19212C>G , LRG_105:g.19212C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1078C>G MANE Select	ENSP00000278407.4:p.Pro360Ala
ENST00000528996.2:c.98C>G	ENSP00000431226.2:p.Thr33Ser
ENST00000531605.2:c.*854C>G	ENSP00000503752.1:n.*854C>G
ENST00000619430.2:c.874C>G	ENSP00000478572.2:p.Pro292Ala
ENST00000676670.1:c.1078C>G	ENSP00000504807.1:p.Pro360Ala
ENST00000676741.1:n.2160C>G
ENST00000677624.1:c.*498C>G	ENSP00000503979.1:n.*498C>G
ENST00000677625.1:c.1030-6C>G	ENSP00000502857.1:n.1030-6C>G
ENST00000677856.1:n.1331C>G
ENST00000677915.1:c.734C>G	ENSP00000503118.1:p.Thr245Ser
ENST00000678533.1:c.*632C>G	ENSP00000503873.1:n.*632C>G
ENST00000678592.1:c.*18C>G	ENSP00000504424.1:n.*18C>G
ENST00000278407.8:c.1078C>G	ENSP00000278407.4:p.Pro360Ala
ENST00000340687.10:c.1030-63C>G	ENSP00000341861.6:n.1030-63C>G
ENST00000378323.8:c.1093C>G	ENSP00000367574.4:p.Pro365Ala
ENST00000378324.6:c.922C>G	ENSP00000367575.2:p.Pro308Ala
ENST00000403558.1:c.1207C>G	ENSP00000384420.1:p.Pro403Ala
ENST00000528996.1:c.279C>G	ENSP00000431226.1:n.279C>G
ENST00000530113.1:n.535C>G
ENST00000531133.5:c.579C>G	ENSP00000435431.1:n.579C>G
ENST00000531797.5:c.*103C>G	ENSP00000432554.1:n.*103C>G
ENST00000619430.1:c.349-140C>G	ENSP00000478572.1:n.349-140C>G
NM_000062.2:c.1078C>G , LRG_105t1:c.1078C>G	NP_000053.2:p.Pro360Ala
NM_001032295.1:c.1078C>G	NP_001027466.1:p.Pro360Ala
NM_000062.3:c.1078C>G MANE Select	NP_000053.2:p.Pro360Ala
NM_001032295.2:c.1078C>G	NP_001027466.1:p.Pro360Ala