Canonical Allele Identifier: CA380690968

Gene: SERPING1

Linked Data

• gnomAD v4: 11-57614576-G-T
• MyVariant Identifiers: chr11:g.57382049G>T (hg19) ; chr11:g.57614576G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614576G>T , CM000673.2:g.57614576G>T	GRCh38
NC_000011.9:g.57382049G>T , CM000673.1:g.57382049G>T	GRCh37
NC_000011.8:g.57138625G>T	NCBI36
NG_009625.1:g.22023G>T , LRG_105:g.22023G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1498G>T MANE Select	ENSP00000278407.4:p.Ala500Ser
ENST00000528996.2:c.*395G>T	ENSP00000431226.2:n.*395G>T
ENST00000531605.2:c.*1274G>T	ENSP00000503752.1:n.*1274G>T
ENST00000619430.2:c.1294G>T	ENSP00000478572.2:p.Ala432Ser
ENST00000676670.1:c.1498G>T	ENSP00000504807.1:p.Ala500Ser
ENST00000676741.1:n.2580G>T
ENST00000677624.1:c.*918G>T	ENSP00000503979.1:n.*918G>T
ENST00000677625.1:c.1444G>T	ENSP00000502857.1:p.Ala482Ser
ENST00000677856.1:n.1751G>T
ENST00000677915.1:c.*395G>T	ENSP00000503118.1:n.*395G>T
ENST00000678533.1:c.*1052G>T	ENSP00000503873.1:n.*1052G>T
ENST00000678592.1:c.*438G>T	ENSP00000504424.1:n.*438G>T
ENST00000278407.8:c.1498G>T	ENSP00000278407.4:p.Ala500Ser
ENST00000340687.10:c.1387G>T	ENSP00000341861.6:p.Ala463Ser
ENST00000378323.8:c.1513G>T	ENSP00000367574.4:p.Ala505Ser
ENST00000378324.6:c.1342G>T	ENSP00000367575.2:p.Ala448Ser
ENST00000403558.1:c.1627G>T	ENSP00000384420.1:p.Ala543Ser
ENST00000528996.1:c.699G>T	ENSP00000431226.1:n.699G>T
ENST00000531133.5:c.999G>T	ENSP00000435431.1:n.999G>T
ENST00000531797.5:c.*523G>T	ENSP00000432554.1:n.*523G>T
ENST00000619430.1:c.629G>T	ENSP00000478572.1:n.629G>T
NM_000062.2:c.1498G>T , LRG_105t1:c.1498G>T	NP_000053.2:p.Ala500Ser
NM_001032295.1:c.1498G>T	NP_001027466.1:p.Ala500Ser
NM_000062.3:c.1498G>T MANE Select	NP_000053.2:p.Ala500Ser
NM_001032295.2:c.1498G>T	NP_001027466.1:p.Ala500Ser