Canonical Allele Identifier: CA380703378

Gene: SERPING1

Linked Data

• gnomAD v4: 11-57611891-A-G
• MyVariant Identifiers: chr11:g.57379364A>G (hg19) ; chr11:g.57611891A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611891A>G , CM000673.2:g.57611891A>G	GRCh38
NC_000011.9:g.57379364A>G , CM000673.1:g.57379364A>G	GRCh37
NC_000011.8:g.57135940A>G	NCBI36
NG_009625.1:g.19338A>G , LRG_105:g.19338A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1204A>G MANE Select	ENSP00000278407.4:p.Lys402Glu
ENST00000528996.2:c.*101A>G	ENSP00000431226.2:n.*101A>G
ENST00000531605.2:c.*980A>G	ENSP00000503752.1:n.*980A>G
ENST00000619430.2:c.1000A>G	ENSP00000478572.2:p.Lys334Glu
ENST00000676670.1:c.1204A>G	ENSP00000504807.1:p.Lys402Glu
ENST00000676741.1:n.2286A>G
ENST00000677624.1:c.*624A>G	ENSP00000503979.1:n.*624A>G
ENST00000677625.1:c.1150A>G	ENSP00000502857.1:p.Lys384Glu
ENST00000677856.1:n.1457A>G
ENST00000677915.1:c.*101A>G	ENSP00000503118.1:n.*101A>G
ENST00000678533.1:c.*758A>G	ENSP00000503873.1:n.*758A>G
ENST00000678592.1:c.*144A>G	ENSP00000504424.1:n.*144A>G
ENST00000278407.8:c.1204A>G	ENSP00000278407.4:p.Lys402Glu
ENST00000340687.10:c.1093A>G	ENSP00000341861.6:p.Lys365Glu
ENST00000378323.8:c.1219A>G	ENSP00000367574.4:p.Lys407Glu
ENST00000378324.6:c.1048A>G	ENSP00000367575.2:p.Lys350Glu
ENST00000403558.1:c.1333A>G	ENSP00000384420.1:p.Lys445Glu
ENST00000528996.1:c.405A>G	ENSP00000431226.1:n.405A>G
ENST00000530113.1:n.661A>G
ENST00000531133.5:c.705A>G	ENSP00000435431.1:n.705A>G
ENST00000531797.5:c.*229A>G	ENSP00000432554.1:n.*229A>G
ENST00000619430.1:c.349-14A>G	ENSP00000478572.1:n.349-14A>G
NM_000062.2:c.1204A>G , LRG_105t1:c.1204A>G	NP_000053.2:p.Lys402Glu
NM_001032295.1:c.1204A>G	NP_001027466.1:p.Lys402Glu
NM_000062.3:c.1204A>G MANE Select	NP_000053.2:p.Lys402Glu
NM_001032295.2:c.1204A>G	NP_001027466.1:p.Lys402Glu