Canonical Allele Identifier: CA380702501

Gene: SERPING1

Linked Data

• dbSNP Id: rs1322345200
• gnomAD v3: 11-57611757-T-C
• gnomAD v4: 11-57611757-T-C
• MyVariant Identifiers: chr11:g.57379230T>C (hg19) ; chr11:g.57611757T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611757T>C , CM000673.2:g.57611757T>C	GRCh38
NC_000011.9:g.57379230T>C , CM000673.1:g.57379230T>C	GRCh37
NC_000011.8:g.57135806T>C	NCBI36
NG_009625.1:g.19204T>C , LRG_105:g.19204T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1070T>C MANE Select	ENSP00000278407.4:p.Ile357Thr
ENST00000528996.2:c.90T>C	ENSP00000431226.2:p.Asp30=
ENST00000531605.2:c.*846T>C	ENSP00000503752.1:n.*846T>C
ENST00000619430.2:c.866T>C	ENSP00000478572.2:p.Ile289Thr
ENST00000676670.1:c.1070T>C	ENSP00000504807.1:p.Ile357Thr
ENST00000676741.1:n.2152T>C
ENST00000677624.1:c.*490T>C	ENSP00000503979.1:n.*490T>C
ENST00000677625.1:c.1030-14T>C	ENSP00000502857.1:n.1030-14T>C
ENST00000677856.1:n.1323T>C
ENST00000677915.1:c.726T>C	ENSP00000503118.1:p.Asp242=
ENST00000678533.1:c.*624T>C	ENSP00000503873.1:n.*624T>C
ENST00000678592.1:c.*10T>C	ENSP00000504424.1:n.*10T>C
ENST00000278407.8:c.1070T>C	ENSP00000278407.4:p.Ile357Thr
ENST00000340687.10:c.1030-71T>C	ENSP00000341861.6:n.1030-71T>C
ENST00000378323.8:c.1085T>C	ENSP00000367574.4:p.Ile362Thr
ENST00000378324.6:c.914T>C	ENSP00000367575.2:p.Ile305Thr
ENST00000403558.1:c.1199T>C	ENSP00000384420.1:p.Ile400Thr
ENST00000528996.1:c.271T>C	ENSP00000431226.1:n.271T>C
ENST00000530113.1:n.527T>C
ENST00000531133.5:c.571T>C	ENSP00000435431.1:n.571T>C
ENST00000531797.5:c.*95T>C	ENSP00000432554.1:n.*95T>C
ENST00000619430.1:c.349-148T>C	ENSP00000478572.1:n.349-148T>C
NM_000062.2:c.1070T>C , LRG_105t1:c.1070T>C	NP_000053.2:p.Ile357Thr
NM_001032295.1:c.1070T>C	NP_001027466.1:p.Ile357Thr
NM_000062.3:c.1070T>C MANE Select	NP_000053.2:p.Ile357Thr
NM_001032295.2:c.1070T>C	NP_001027466.1:p.Ile357Thr