Canonical Allele Identifier: CA380702845

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57379286C>T (hg19) ; chr11:g.57611813C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611813C>T , CM000673.2:g.57611813C>T	GRCh38
NC_000011.9:g.57379286C>T , CM000673.1:g.57379286C>T	GRCh37
NC_000011.8:g.57135862C>T	NCBI36
NG_009625.1:g.19260C>T , LRG_105:g.19260C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1126C>T MANE Select	ENSP00000278407.4:p.Pro376Ser
ENST00000528996.2:c.*23C>T	ENSP00000431226.2:n.*23C>T
ENST00000531605.2:c.*902C>T	ENSP00000503752.1:n.*902C>T
ENST00000619430.2:c.922C>T	ENSP00000478572.2:p.Pro308Ser
ENST00000676670.1:c.1126C>T	ENSP00000504807.1:p.Pro376Ser
ENST00000676741.1:n.2208C>T
ENST00000677624.1:c.*546C>T	ENSP00000503979.1:n.*546C>T
ENST00000677625.1:c.1072C>T	ENSP00000502857.1:p.Pro358Ser
ENST00000677856.1:n.1379C>T
ENST00000677915.1:c.*23C>T	ENSP00000503118.1:n.*23C>T
ENST00000678533.1:c.*680C>T	ENSP00000503873.1:n.*680C>T
ENST00000678592.1:c.*66C>T	ENSP00000504424.1:n.*66C>T
ENST00000278407.8:c.1126C>T	ENSP00000278407.4:p.Pro376Ser
ENST00000340687.10:c.1030-15C>T	ENSP00000341861.6:n.1030-15C>T
ENST00000378323.8:c.1141C>T	ENSP00000367574.4:p.Pro381Ser
ENST00000378324.6:c.970C>T	ENSP00000367575.2:p.Pro324Ser
ENST00000403558.1:c.1255C>T	ENSP00000384420.1:p.Pro419Ser
ENST00000528996.1:c.327C>T	ENSP00000431226.1:n.327C>T
ENST00000530113.1:n.583C>T
ENST00000531133.5:c.627C>T	ENSP00000435431.1:n.627C>T
ENST00000531797.5:c.*151C>T	ENSP00000432554.1:n.*151C>T
ENST00000619430.1:c.349-92C>T	ENSP00000478572.1:n.349-92C>T
NM_000062.2:c.1126C>T , LRG_105t1:c.1126C>T	NP_000053.2:p.Pro376Ser
NM_001032295.1:c.1126C>T	NP_001027466.1:p.Pro376Ser
NM_000062.3:c.1126C>T MANE Select	NP_000053.2:p.Pro376Ser
NM_001032295.2:c.1126C>T	NP_001027466.1:p.Pro376Ser