Canonical Allele Identifier: CA2613603968

Gene: SERPING1

Linked Data

• gnomAD v4: 11-57614733-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614733G>C , CM000673.2:g.57614733G>C	GRCh38
NC_000011.9:g.57382206G>C , CM000673.1:g.57382206G>C	GRCh37
NC_000011.8:g.57138782G>C	NCBI36
NG_009625.1:g.22180G>C , LRG_105:g.22180G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.*152G>C MANE Select	ENSP00000278407.4:n.*152G>C
ENST00000528996.2:c.*552G>C	ENSP00000431226.2:n.*552G>C
ENST00000531605.2:c.*1431G>C	ENSP00000503752.1:n.*1431G>C
ENST00000619430.2:c.*152G>C	ENSP00000478572.2:n.*152G>C
ENST00000676670.1:c.*15+137G>C	ENSP00000504807.1:n.*15+137G>C
ENST00000676741.1:n.2737G>C
ENST00000677624.1:c.*1075G>C	ENSP00000503979.1:n.*1075G>C
ENST00000677625.1:c.*152G>C	ENSP00000502857.1:n.*152G>C
ENST00000677856.1:n.1908G>C
ENST00000677915.1:c.*552G>C	ENSP00000503118.1:n.*552G>C
ENST00000678533.1:c.*1072+137G>C	ENSP00000503873.1:n.*1072+137G>C
ENST00000678592.1:c.*595G>C	ENSP00000504424.1:n.*595G>C
ENST00000278407.8:c.*152G>C	ENSP00000278407.4:n.*152G>C
ENST00000340687.10:c.*152G>C	ENSP00000341861.6:n.*152G>C
ENST00000378323.8:c.*152G>C	ENSP00000367574.4:n.*152G>C
ENST00000378324.6:c.*152G>C	ENSP00000367575.2:n.*152G>C
ENST00000403558.1:c.*152G>C	ENSP00000384420.1:n.*152G>C
ENST00000528996.1:c.856G>C	ENSP00000431226.1:n.856G>C
ENST00000531797.5:c.*680G>C	ENSP00000432554.1:n.*680G>C
NM_000062.2:c.*152G>C , LRG_105t1:c.*152G>C	NP_000053.2:n.*152G>C
NM_001032295.1:c.*152G>C	NP_001027466.1:n.*152G>C
NM_000062.3:c.*152G>C MANE Select	NP_000053.2:n.*152G>C
NM_001032295.2:c.*152G>C	NP_001027466.1:n.*152G>C