Canonical Allele Identifier: CA380690315

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381837G>C (hg19) ; chr11:g.57614364G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614364G>C , CM000673.2:g.57614364G>C	GRCh38
NC_000011.9:g.57381837G>C , CM000673.1:g.57381837G>C	GRCh37
NC_000011.8:g.57138413G>C	NCBI36
NG_009625.1:g.21811G>C , LRG_105:g.21811G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1286G>C MANE Select	ENSP00000278407.4:p.Gly429Ala
ENST00000528996.2:c.*183G>C	ENSP00000431226.2:n.*183G>C
ENST00000531605.2:c.*1062G>C	ENSP00000503752.1:n.*1062G>C
ENST00000619430.2:c.1082G>C	ENSP00000478572.2:p.Gly361Ala
ENST00000676670.1:c.1286G>C	ENSP00000504807.1:p.Gly429Ala
ENST00000676741.1:n.2368G>C
ENST00000677624.1:c.*706G>C	ENSP00000503979.1:n.*706G>C
ENST00000677625.1:c.1232G>C	ENSP00000502857.1:p.Gly411Ala
ENST00000677856.1:n.1539G>C
ENST00000677915.1:c.*183G>C	ENSP00000503118.1:n.*183G>C
ENST00000678533.1:c.*840G>C	ENSP00000503873.1:n.*840G>C
ENST00000678592.1:c.*226G>C	ENSP00000504424.1:n.*226G>C
ENST00000278407.8:c.1286G>C	ENSP00000278407.4:p.Gly429Ala
ENST00000340687.10:c.1175G>C	ENSP00000341861.6:p.Gly392Ala
ENST00000378323.8:c.1301G>C	ENSP00000367574.4:p.Gly434Ala
ENST00000378324.6:c.1130G>C	ENSP00000367575.2:p.Gly377Ala
ENST00000403558.1:c.1415G>C	ENSP00000384420.1:p.Gly472Ala
ENST00000528996.1:c.487G>C	ENSP00000431226.1:n.487G>C
ENST00000530113.1:n.743G>C
ENST00000531133.5:c.787G>C	ENSP00000435431.1:n.787G>C
ENST00000531797.5:c.*311G>C	ENSP00000432554.1:n.*311G>C
ENST00000619430.1:c.417G>C	ENSP00000478572.1:n.417G>C
NM_000062.2:c.1286G>C , LRG_105t1:c.1286G>C	NP_000053.2:p.Gly429Ala
NM_001032295.1:c.1286G>C	NP_001027466.1:p.Gly429Ala
NM_000062.3:c.1286G>C MANE Select	NP_000053.2:p.Gly429Ala
NM_001032295.2:c.1286G>C	NP_001027466.1:p.Gly429Ala