Canonical Allele Identifier: CA6008061

Gene: SERPING1

Linked Data

• dbSNP Id: rs564416281
• ExAC: 11:57367876 A / C
• gnomAD v2: 11-57367876-A-C
• gnomAD v3: 11-57600403-A-C
• gnomAD v4: 11-57600403-A-C
• MyVariant Identifiers: chr11:g.57367876A>C (hg19) ; chr11:g.57600403A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57600403A>C , CM000673.2:g.57600403A>C	GRCh38
NC_000011.9:g.57367876A>C , CM000673.1:g.57367876A>C	GRCh37
NC_000011.8:g.57124452A>C	NCBI36
NG_009625.1:g.7850A>C , LRG_105:g.7850A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.550+26A>C MANE Select	ENSP00000278407.4:n.550+26A>C
ENST00000528996.2:c.58+2075A>C	ENSP00000431226.2:n.58+2075A>C
ENST00000531605.2:c.52-1632A>C	ENSP00000503752.1:n.52-1632A>C
ENST00000619430.2:c.550+26A>C	ENSP00000478572.2:n.550+26A>C
ENST00000676670.1:c.550+26A>C	ENSP00000504807.1:n.550+26A>C
ENST00000676741.1:n.1632+26A>C
ENST00000677275.1:n.537+26A>C
ENST00000677624.1:c.550+26A>C	ENSP00000503979.1:n.550+26A>C
ENST00000677625.1:c.550+26A>C	ENSP00000502857.1:n.550+26A>C
ENST00000677856.1:n.609+26A>C
ENST00000677915.1:c.550+26A>C	ENSP00000503118.1:n.550+26A>C
ENST00000678533.1:c.52-1632A>C	ENSP00000503873.1:n.52-1632A>C
ENST00000678592.1:c.550+26A>C	ENSP00000504424.1:n.550+26A>C
ENST00000278407.8:c.550+26A>C	ENSP00000278407.4:n.550+26A>C
ENST00000340687.10:c.550+26A>C	ENSP00000341861.6:n.550+26A>C
ENST00000378323.8:c.565+26A>C	ENSP00000367574.4:n.565+26A>C
ENST00000378324.6:c.394+26A>C	ENSP00000367575.2:n.394+26A>C
ENST00000403558.1:c.652+26A>C	ENSP00000384420.1:n.652+26A>C
ENST00000531133.5:c.52-1632A>C	ENSP00000435431.1:n.52-1632A>C
ENST00000531797.5:c.52-1632A>C	ENSP00000432554.1:n.52-1632A>C
ENST00000619430.1:c.348+228A>C	ENSP00000478572.1:n.348+228A>C
NM_000062.2:c.550+26A>C , LRG_105t1:c.550+26A>C	NP_000053.2:n.550+26A>C
NM_001032295.1:c.550+26A>C	NP_001027466.1:n.550+26A>C
NM_000062.3:c.550+26A>C MANE Select	NP_000053.2:n.550+26A>C
NM_001032295.2:c.550+26A>C	NP_001027466.1:n.550+26A>C