Canonical Allele Identifier: CA380695068

Gene: SERPING1

Linked Data

• dbSNP Id: rs1945331592
• gnomAD v3: 11-57600126-T-C
• gnomAD v4: 11-57600126-T-C
• MyVariant Identifiers: chr11:g.57367599T>C (hg19) ; chr11:g.57600126T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57600126T>C , CM000673.2:g.57600126T>C	GRCh38
NC_000011.9:g.57367599T>C , CM000673.1:g.57367599T>C	GRCh37
NC_000011.8:g.57124175T>C	NCBI36
NG_009625.1:g.7573T>C , LRG_105:g.7573T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.299T>C MANE Select	ENSP00000278407.4:p.Ile100Thr
ENST00000528996.2:c.58+1798T>C	ENSP00000431226.2:n.58+1798T>C
ENST00000531605.2:c.51+1805T>C	ENSP00000503752.1:n.51+1805T>C
ENST00000619430.2:c.299T>C	ENSP00000478572.2:p.Ile100Thr
ENST00000676670.1:c.299T>C	ENSP00000504807.1:p.Ile100Thr
ENST00000676741.1:n.1381T>C
ENST00000677275.1:n.286T>C
ENST00000677624.1:c.299T>C	ENSP00000503979.1:p.Ile100Thr
ENST00000677625.1:c.299T>C	ENSP00000502857.1:p.Ile100Thr
ENST00000677856.1:n.358T>C
ENST00000677915.1:c.299T>C	ENSP00000503118.1:p.Ile100Thr
ENST00000678533.1:c.51+1805T>C	ENSP00000503873.1:n.51+1805T>C
ENST00000678592.1:c.299T>C	ENSP00000504424.1:p.Ile100Thr
ENST00000278407.8:c.299T>C	ENSP00000278407.4:p.Ile100Thr
ENST00000340687.10:c.299T>C	ENSP00000341861.6:p.Ile100Thr
ENST00000378323.8:c.314T>C	ENSP00000367574.4:p.Ile105Thr
ENST00000378324.6:c.143T>C	ENSP00000367575.2:p.Ile48Thr
ENST00000403558.1:c.401T>C	ENSP00000384420.1:p.Ile134Thr
ENST00000405496.5:c.299T>C	ENSP00000384561.1:p.Ile100Thr
ENST00000531133.5:c.51+1805T>C	ENSP00000435431.1:n.51+1805T>C
ENST00000531797.5:c.51+1805T>C	ENSP00000432554.1:n.51+1805T>C
ENST00000619430.1:c.299T>C	ENSP00000478572.1:p.Ile100Thr
NM_000062.2:c.299T>C , LRG_105t1:c.299T>C	NP_000053.2:p.Ile100Thr
NM_001032295.1:c.299T>C	NP_001027466.1:p.Ile100Thr
NM_000062.3:c.299T>C MANE Select	NP_000053.2:p.Ile100Thr
NM_001032295.2:c.299T>C	NP_001027466.1:p.Ile100Thr