Canonical Allele Identifier: CA2613604043

Gene: SERPING1

Linked Data

• gnomAD v4: 11-57614759-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614759A>C , CM000673.2:g.57614759A>C	GRCh38
NC_000011.9:g.57382232A>C , CM000673.1:g.57382232A>C	GRCh37
NC_000011.8:g.57138808A>C	NCBI36
NG_009625.1:g.22206A>C , LRG_105:g.22206A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.*178A>C MANE Select	ENSP00000278407.4:n.*178A>C
ENST00000528996.2:c.*578A>C	ENSP00000431226.2:n.*578A>C
ENST00000531605.2:c.*1457A>C	ENSP00000503752.1:n.*1457A>C
ENST00000619430.2:c.*178A>C	ENSP00000478572.2:n.*178A>C
ENST00000676670.1:c.*15+163A>C	ENSP00000504807.1:n.*15+163A>C
ENST00000676741.1:n.2763A>C
ENST00000677624.1:c.*1101A>C	ENSP00000503979.1:n.*1101A>C
ENST00000677625.1:c.*178A>C	ENSP00000502857.1:n.*178A>C
ENST00000677856.1:n.1934A>C
ENST00000677915.1:c.*578A>C	ENSP00000503118.1:n.*578A>C
ENST00000678533.1:c.*1072+163A>C	ENSP00000503873.1:n.*1072+163A>C
ENST00000678592.1:c.*621A>C	ENSP00000504424.1:n.*621A>C
ENST00000278407.8:c.*178A>C	ENSP00000278407.4:n.*178A>C
ENST00000340687.10:c.*178A>C	ENSP00000341861.6:n.*178A>C
ENST00000378324.6:c.*178A>C	ENSP00000367575.2:n.*178A>C
ENST00000403558.1:c.*178A>C	ENSP00000384420.1:n.*178A>C
ENST00000528996.1:c.882A>C	ENSP00000431226.1:n.882A>C
ENST00000531797.5:c.*706A>C	ENSP00000432554.1:n.*706A>C
NM_000062.2:c.*178A>C , LRG_105t1:c.*178A>C	NP_000053.2:n.*178A>C
NM_001032295.1:c.*178A>C	NP_001027466.1:n.*178A>C
NM_000062.3:c.*178A>C MANE Select	NP_000053.2:n.*178A>C
NM_001032295.2:c.*178A>C	NP_001027466.1:n.*178A>C