Canonical Allele Identifier: CA380690326

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381840T>C (hg19) ; chr11:g.57614367T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614367T>C , CM000673.2:g.57614367T>C	GRCh38
NC_000011.9:g.57381840T>C , CM000673.1:g.57381840T>C	GRCh37
NC_000011.8:g.57138416T>C	NCBI36
NG_009625.1:g.21814T>C , LRG_105:g.21814T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1289T>C MANE Select	ENSP00000278407.4:p.Leu430Pro
ENST00000528996.2:c.*186T>C	ENSP00000431226.2:n.*186T>C
ENST00000531605.2:c.*1065T>C	ENSP00000503752.1:n.*1065T>C
ENST00000619430.2:c.1085T>C	ENSP00000478572.2:p.Leu362Pro
ENST00000676670.1:c.1289T>C	ENSP00000504807.1:p.Leu430Pro
ENST00000676741.1:n.2371T>C
ENST00000677624.1:c.*709T>C	ENSP00000503979.1:n.*709T>C
ENST00000677625.1:c.1235T>C	ENSP00000502857.1:p.Leu412Pro
ENST00000677856.1:n.1542T>C
ENST00000677915.1:c.*186T>C	ENSP00000503118.1:n.*186T>C
ENST00000678533.1:c.*843T>C	ENSP00000503873.1:n.*843T>C
ENST00000678592.1:c.*229T>C	ENSP00000504424.1:n.*229T>C
ENST00000278407.8:c.1289T>C	ENSP00000278407.4:p.Leu430Pro
ENST00000340687.10:c.1178T>C	ENSP00000341861.6:p.Leu393Pro
ENST00000378323.8:c.1304T>C	ENSP00000367574.4:p.Leu435Pro
ENST00000378324.6:c.1133T>C	ENSP00000367575.2:p.Leu378Pro
ENST00000403558.1:c.1418T>C	ENSP00000384420.1:p.Leu473Pro
ENST00000528996.1:c.490T>C	ENSP00000431226.1:n.490T>C
ENST00000530113.1:n.746T>C
ENST00000531133.5:c.790T>C	ENSP00000435431.1:n.790T>C
ENST00000531797.5:c.*314T>C	ENSP00000432554.1:n.*314T>C
ENST00000619430.1:c.420T>C	ENSP00000478572.1:n.420T>C
NM_000062.2:c.1289T>C , LRG_105t1:c.1289T>C	NP_000053.2:p.Leu430Pro
NM_001032295.1:c.1289T>C	NP_001027466.1:p.Leu430Pro
NM_000062.3:c.1289T>C MANE Select	NP_000053.2:p.Leu430Pro
NM_001032295.2:c.1289T>C	NP_001027466.1:p.Leu430Pro