Canonical Allele Identifier: CA2613604011

Gene: SERPING1

Linked Data

• gnomAD v4: 11-57614747-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614747T>C , CM000673.2:g.57614747T>C	GRCh38
NC_000011.9:g.57382220T>C , CM000673.1:g.57382220T>C	GRCh37
NC_000011.8:g.57138796T>C	NCBI36
NG_009625.1:g.22194T>C , LRG_105:g.22194T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.*166T>C MANE Select	ENSP00000278407.4:n.*166T>C
ENST00000528996.2:c.*566T>C	ENSP00000431226.2:n.*566T>C
ENST00000531605.2:c.*1445T>C	ENSP00000503752.1:n.*1445T>C
ENST00000619430.2:c.*166T>C	ENSP00000478572.2:n.*166T>C
ENST00000676670.1:c.*15+151T>C	ENSP00000504807.1:n.*15+151T>C
ENST00000676741.1:n.2751T>C
ENST00000677624.1:c.*1089T>C	ENSP00000503979.1:n.*1089T>C
ENST00000677625.1:c.*166T>C	ENSP00000502857.1:n.*166T>C
ENST00000677856.1:n.1922T>C
ENST00000677915.1:c.*566T>C	ENSP00000503118.1:n.*566T>C
ENST00000678533.1:c.*1072+151T>C	ENSP00000503873.1:n.*1072+151T>C
ENST00000678592.1:c.*609T>C	ENSP00000504424.1:n.*609T>C
ENST00000278407.8:c.*166T>C	ENSP00000278407.4:n.*166T>C
ENST00000340687.10:c.*166T>C	ENSP00000341861.6:n.*166T>C
ENST00000378324.6:c.*166T>C	ENSP00000367575.2:n.*166T>C
ENST00000403558.1:c.*166T>C	ENSP00000384420.1:n.*166T>C
ENST00000528996.1:c.870T>C	ENSP00000431226.1:n.870T>C
ENST00000531797.5:c.*694T>C	ENSP00000432554.1:n.*694T>C
NM_000062.2:c.*166T>C , LRG_105t1:c.*166T>C	NP_000053.2:n.*166T>C
NM_001032295.1:c.*166T>C	NP_001027466.1:n.*166T>C
NM_000062.3:c.*166T>C MANE Select	NP_000053.2:n.*166T>C
NM_001032295.2:c.*166T>C	NP_001027466.1:n.*166T>C