Canonical Allele Identifier: CA380690974

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57382053G>C (hg19) ; chr11:g.57614580G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614580G>C , CM000673.2:g.57614580G>C	GRCh38
NC_000011.9:g.57382053G>C , CM000673.1:g.57382053G>C	GRCh37
NC_000011.8:g.57138629G>C	NCBI36
NG_009625.1:g.22027G>C , LRG_105:g.22027G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1502G>C MANE Select	ENSP00000278407.4:p.Ter501Ser
ENST00000528996.2:c.*399G>C	ENSP00000431226.2:n.*399G>C
ENST00000531605.2:c.*1278G>C	ENSP00000503752.1:n.*1278G>C
ENST00000619430.2:c.1298G>C	ENSP00000478572.2:p.Ter433Ser
ENST00000676670.1:c.1502G>C	ENSP00000504807.1:p.Ter501Ser
ENST00000676741.1:n.2584G>C
ENST00000677624.1:c.*922G>C	ENSP00000503979.1:n.*922G>C
ENST00000677625.1:c.1448G>C	ENSP00000502857.1:p.Ter483Ser
ENST00000677856.1:n.1755G>C
ENST00000677915.1:c.*399G>C	ENSP00000503118.1:n.*399G>C
ENST00000678533.1:c.*1056G>C	ENSP00000503873.1:n.*1056G>C
ENST00000678592.1:c.*442G>C	ENSP00000504424.1:n.*442G>C
ENST00000278407.8:c.1502G>C	ENSP00000278407.4:p.Ter501Ser
ENST00000340687.10:c.1391G>C	ENSP00000341861.6:p.Ter464Ser
ENST00000378323.8:c.1517G>C	ENSP00000367574.4:p.Ter506Ser
ENST00000378324.6:c.1346G>C	ENSP00000367575.2:p.Ter449Ser
ENST00000403558.1:c.1631G>C	ENSP00000384420.1:p.Ter544Ser
ENST00000528996.1:c.703G>C	ENSP00000431226.1:n.703G>C
ENST00000531133.5:c.1003G>C	ENSP00000435431.1:n.1003G>C
ENST00000531797.5:c.*527G>C	ENSP00000432554.1:n.*527G>C
ENST00000619430.1:c.633G>C	ENSP00000478572.1:n.633G>C
NM_000062.2:c.1502G>C , LRG_105t1:c.1502G>C	NP_000053.2:p.Ter501Ser
NM_001032295.1:c.1502G>C	NP_001027466.1:p.Ter501Ser
NM_000062.3:c.1502G>C MANE Select	NP_000053.2:p.Ter501Ser
NM_001032295.2:c.1502G>C	NP_001027466.1:p.Ter501Ser