Canonical Allele Identifier: CA380690604

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381896C>G (hg19) ; chr11:g.57614423C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614423C>G , CM000673.2:g.57614423C>G	GRCh38
NC_000011.9:g.57381896C>G , CM000673.1:g.57381896C>G	GRCh37
NC_000011.8:g.57138472C>G	NCBI36
NG_009625.1:g.21870C>G , LRG_105:g.21870C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1345C>G MANE Select	ENSP00000278407.4:p.Leu449Val
ENST00000528996.2:c.*242C>G	ENSP00000431226.2:n.*242C>G
ENST00000531605.2:c.*1121C>G	ENSP00000503752.1:n.*1121C>G
ENST00000619430.2:c.1141C>G	ENSP00000478572.2:p.Leu381Val
ENST00000676670.1:c.1345C>G	ENSP00000504807.1:p.Leu449Val
ENST00000676741.1:n.2427C>G
ENST00000677624.1:c.*765C>G	ENSP00000503979.1:n.*765C>G
ENST00000677625.1:c.1291C>G	ENSP00000502857.1:p.Leu431Val
ENST00000677856.1:n.1598C>G
ENST00000677915.1:c.*242C>G	ENSP00000503118.1:n.*242C>G
ENST00000678533.1:c.*899C>G	ENSP00000503873.1:n.*899C>G
ENST00000678592.1:c.*285C>G	ENSP00000504424.1:n.*285C>G
ENST00000278407.8:c.1345C>G	ENSP00000278407.4:p.Leu449Val
ENST00000340687.10:c.1234C>G	ENSP00000341861.6:p.Leu412Val
ENST00000378323.8:c.1360C>G	ENSP00000367574.4:p.Leu454Val
ENST00000378324.6:c.1189C>G	ENSP00000367575.2:p.Leu397Val
ENST00000403558.1:c.1474C>G	ENSP00000384420.1:p.Leu492Val
ENST00000528996.1:c.546C>G	ENSP00000431226.1:n.546C>G
ENST00000530113.1:n.802C>G
ENST00000531133.5:c.846C>G	ENSP00000435431.1:n.846C>G
ENST00000531797.5:c.*370C>G	ENSP00000432554.1:n.*370C>G
ENST00000619430.1:c.476C>G	ENSP00000478572.1:n.476C>G
NM_000062.2:c.1345C>G , LRG_105t1:c.1345C>G	NP_000053.2:p.Leu449Val
NM_001032295.1:c.1345C>G	NP_001027466.1:p.Leu449Val
NM_000062.3:c.1345C>G MANE Select	NP_000053.2:p.Leu449Val
NM_001032295.2:c.1345C>G	NP_001027466.1:p.Leu449Val