Canonical Allele Identifier: CA380702463

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57379224T>C (hg19) ; chr11:g.57611751T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611751T>C , CM000673.2:g.57611751T>C	GRCh38
NC_000011.9:g.57379224T>C , CM000673.1:g.57379224T>C	GRCh37
NC_000011.8:g.57135800T>C	NCBI36
NG_009625.1:g.19198T>C , LRG_105:g.19198T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1064T>C MANE Select	ENSP00000278407.4:p.Leu355Ser
ENST00000528996.2:c.84T>C	ENSP00000431226.2:p.Phe28=
ENST00000531605.2:c.*840T>C	ENSP00000503752.1:n.*840T>C
ENST00000619430.2:c.860T>C	ENSP00000478572.2:p.Leu287Ser
ENST00000676670.1:c.1064T>C	ENSP00000504807.1:p.Leu355Ser
ENST00000676741.1:n.2146T>C
ENST00000677624.1:c.*484T>C	ENSP00000503979.1:n.*484T>C
ENST00000677625.1:c.1030-20T>C	ENSP00000502857.1:n.1030-20T>C
ENST00000677856.1:n.1317T>C
ENST00000677915.1:c.720T>C	ENSP00000503118.1:p.Phe240=
ENST00000678533.1:c.*618T>C	ENSP00000503873.1:n.*618T>C
ENST00000678592.1:c.*4T>C	ENSP00000504424.1:n.*4T>C
ENST00000278407.8:c.1064T>C	ENSP00000278407.4:p.Leu355Ser
ENST00000340687.10:c.1030-77T>C	ENSP00000341861.6:n.1030-77T>C
ENST00000378323.8:c.1079T>C	ENSP00000367574.4:p.Leu360Ser
ENST00000378324.6:c.908T>C	ENSP00000367575.2:p.Leu303Ser
ENST00000403558.1:c.1193T>C	ENSP00000384420.1:p.Leu398Ser
ENST00000528996.1:c.265T>C	ENSP00000431226.1:n.265T>C
ENST00000530113.1:n.521T>C
ENST00000531133.5:c.565T>C	ENSP00000435431.1:n.565T>C
ENST00000531797.5:c.*89T>C	ENSP00000432554.1:n.*89T>C
ENST00000619430.1:c.349-154T>C	ENSP00000478572.1:n.349-154T>C
NM_000062.2:c.1064T>C , LRG_105t1:c.1064T>C	NP_000053.2:p.Leu355Ser
NM_001032295.1:c.1064T>C	NP_001027466.1:p.Leu355Ser
NM_000062.3:c.1064T>C MANE Select	NP_000053.2:p.Leu355Ser
NM_001032295.2:c.1064T>C	NP_001027466.1:p.Leu355Ser