Canonical Allele Identifier: CA474565937
Gene: SERPING1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.57369548C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57602075C>G , CM000673.2:g.57602075C>G GRCh38
NC_000011.9:g.57369548C>G , CM000673.1:g.57369548C>G GRCh37
NC_000011.8:g.57126124C>G NCBI36
NG_009625.1:g.9522C>G , LRG_105:g.9522C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.591C>G MANE Select ENSP00000278407.4:p.Leu197=
ENST00000528996.2:c.58+3747C>G ENSP00000431226.2:n.58+3747C>G
ENST00000531605.2:c.92C>G ENSP00000503752.1:p.Ser31Cys
ENST00000619430.2:c.591C>G ENSP00000478572.2:p.Leu197=
ENST00000676670.1:c.591C>G ENSP00000504807.1:p.Leu197=
ENST00000676741.1:n.1673C>G
ENST00000677275.1:n.578C>G
ENST00000677624.1:c.591C>G ENSP00000503979.1:p.Leu197=
ENST00000677625.1:c.591C>G ENSP00000502857.1:p.Leu197=
ENST00000677856.1:n.650C>G
ENST00000677915.1:c.591C>G ENSP00000503118.1:p.Leu197=
ENST00000678533.1:c.92C>G ENSP00000503873.1:p.Ser31Cys
ENST00000678592.1:c.591C>G ENSP00000504424.1:p.Leu197=
ENST00000278407.8:c.591C>G ENSP00000278407.4:p.Leu197=
ENST00000340687.10:c.591C>G ENSP00000341861.6:p.Leu197=
ENST00000378323.8:c.606C>G ENSP00000367574.4:p.Leu202=
ENST00000378324.6:c.435C>G ENSP00000367575.2:p.Leu145=
ENST00000403558.1:c.693C>G ENSP00000384420.1:p.Leu231=
ENST00000531133.5:c.92C>G ENSP00000435431.1:p.Ser31Cys
ENST00000531605.1:n.31C>G
ENST00000531797.5:c.92C>G ENSP00000432554.1:p.Ser31Cys
ENST00000619430.1:c.348+1900C>G ENSP00000478572.1:n.348+1900C>G
NM_000062.2:c.591C>G , LRG_105t1:c.591C>G NP_000053.2:p.Leu197=
NM_001032295.1:c.591C>G NP_001027466.1:p.Leu197=
NM_000062.3:c.591C>G MANE Select NP_000053.2:p.Leu197=
NM_001032295.2:c.591C>G NP_001027466.1:p.Leu197=