Canonical Allele Identifier: CA380690972

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57382052T>C (hg19) ; chr11:g.57614579T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614579T>C , CM000673.2:g.57614579T>C	GRCh38
NC_000011.9:g.57382052T>C , CM000673.1:g.57382052T>C	GRCh37
NC_000011.8:g.57138628T>C	NCBI36
NG_009625.1:g.22026T>C , LRG_105:g.22026T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1501T>C MANE Select	ENSP00000278407.4:p.Ter501Arg
ENST00000528996.2:c.*398T>C	ENSP00000431226.2:n.*398T>C
ENST00000531605.2:c.*1277T>C	ENSP00000503752.1:n.*1277T>C
ENST00000619430.2:c.1297T>C	ENSP00000478572.2:p.Ter433Arg
ENST00000676670.1:c.1501T>C	ENSP00000504807.1:p.Ter501Arg
ENST00000676741.1:n.2583T>C
ENST00000677624.1:c.*921T>C	ENSP00000503979.1:n.*921T>C
ENST00000677625.1:c.1447T>C	ENSP00000502857.1:p.Ter483Arg
ENST00000677856.1:n.1754T>C
ENST00000677915.1:c.*398T>C	ENSP00000503118.1:n.*398T>C
ENST00000678533.1:c.*1055T>C	ENSP00000503873.1:n.*1055T>C
ENST00000678592.1:c.*441T>C	ENSP00000504424.1:n.*441T>C
ENST00000278407.8:c.1501T>C	ENSP00000278407.4:p.Ter501Arg
ENST00000340687.10:c.1390T>C	ENSP00000341861.6:p.Ter464Arg
ENST00000378323.8:c.1516T>C	ENSP00000367574.4:p.Ter506Arg
ENST00000378324.6:c.1345T>C	ENSP00000367575.2:p.Ter449Arg
ENST00000403558.1:c.1630T>C	ENSP00000384420.1:p.Ter544Arg
ENST00000528996.1:c.702T>C	ENSP00000431226.1:n.702T>C
ENST00000531133.5:c.1002T>C	ENSP00000435431.1:n.1002T>C
ENST00000531797.5:c.*526T>C	ENSP00000432554.1:n.*526T>C
ENST00000619430.1:c.632T>C	ENSP00000478572.1:n.632T>C
NM_000062.2:c.1501T>C , LRG_105t1:c.1501T>C	NP_000053.2:p.Ter501Arg
NM_001032295.1:c.1501T>C	NP_001027466.1:p.Ter501Arg
NM_000062.3:c.1501T>C MANE Select	NP_000053.2:p.Ter501Arg
NM_001032295.2:c.1501T>C	NP_001027466.1:p.Ter501Arg