Canonical Allele Identifier: CA380690531

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381879A>T (hg19) ; chr11:g.57614406A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614406A>T , CM000673.2:g.57614406A>T	GRCh38
NC_000011.9:g.57381879A>T , CM000673.1:g.57381879A>T	GRCh37
NC_000011.8:g.57138455A>T	NCBI36
NG_009625.1:g.21853A>T , LRG_105:g.21853A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1328A>T MANE Select	ENSP00000278407.4:p.His443Leu
ENST00000528996.2:c.*225A>T	ENSP00000431226.2:n.*225A>T
ENST00000531605.2:c.*1104A>T	ENSP00000503752.1:n.*1104A>T
ENST00000619430.2:c.1124A>T	ENSP00000478572.2:p.His375Leu
ENST00000676670.1:c.1328A>T	ENSP00000504807.1:p.His443Leu
ENST00000676741.1:n.2410A>T
ENST00000677624.1:c.*748A>T	ENSP00000503979.1:n.*748A>T
ENST00000677625.1:c.1274A>T	ENSP00000502857.1:p.His425Leu
ENST00000677856.1:n.1581A>T
ENST00000677915.1:c.*225A>T	ENSP00000503118.1:n.*225A>T
ENST00000678533.1:c.*882A>T	ENSP00000503873.1:n.*882A>T
ENST00000678592.1:c.*268A>T	ENSP00000504424.1:n.*268A>T
ENST00000278407.8:c.1328A>T	ENSP00000278407.4:p.His443Leu
ENST00000340687.10:c.1217A>T	ENSP00000341861.6:p.His406Leu
ENST00000378323.8:c.1343A>T	ENSP00000367574.4:p.His448Leu
ENST00000378324.6:c.1172A>T	ENSP00000367575.2:p.His391Leu
ENST00000403558.1:c.1457A>T	ENSP00000384420.1:p.His486Leu
ENST00000528996.1:c.529A>T	ENSP00000431226.1:n.529A>T
ENST00000530113.1:n.785A>T
ENST00000531133.5:c.829A>T	ENSP00000435431.1:n.829A>T
ENST00000531797.5:c.*353A>T	ENSP00000432554.1:n.*353A>T
ENST00000619430.1:c.459A>T	ENSP00000478572.1:n.459A>T
NM_000062.2:c.1328A>T , LRG_105t1:c.1328A>T	NP_000053.2:p.His443Leu
NM_001032295.1:c.1328A>T	NP_001027466.1:p.His443Leu
NM_000062.3:c.1328A>T MANE Select	NP_000053.2:p.His443Leu
NM_001032295.2:c.1328A>T	NP_001027466.1:p.His443Leu