Canonical Allele Identifier: CA380702490

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57379229A>C (hg19) ; chr11:g.57611756A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611756A>C , CM000673.2:g.57611756A>C	GRCh38
NC_000011.9:g.57379229A>C , CM000673.1:g.57379229A>C	GRCh37
NC_000011.8:g.57135805A>C	NCBI36
NG_009625.1:g.19203A>C , LRG_105:g.19203A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1069A>C MANE Select	ENSP00000278407.4:p.Ile357Leu
ENST00000528996.2:c.89A>C	ENSP00000431226.2:p.Asp30Ala
ENST00000531605.2:c.*845A>C	ENSP00000503752.1:n.*845A>C
ENST00000619430.2:c.865A>C	ENSP00000478572.2:p.Ile289Leu
ENST00000676670.1:c.1069A>C	ENSP00000504807.1:p.Ile357Leu
ENST00000676741.1:n.2151A>C
ENST00000677624.1:c.*489A>C	ENSP00000503979.1:n.*489A>C
ENST00000677625.1:c.1030-15A>C	ENSP00000502857.1:n.1030-15A>C
ENST00000677856.1:n.1322A>C
ENST00000677915.1:c.725A>C	ENSP00000503118.1:p.Asp242Ala
ENST00000678533.1:c.*623A>C	ENSP00000503873.1:n.*623A>C
ENST00000678592.1:c.*9A>C	ENSP00000504424.1:n.*9A>C
ENST00000278407.8:c.1069A>C	ENSP00000278407.4:p.Ile357Leu
ENST00000340687.10:c.1030-72A>C	ENSP00000341861.6:n.1030-72A>C
ENST00000378323.8:c.1084A>C	ENSP00000367574.4:p.Ile362Leu
ENST00000378324.6:c.913A>C	ENSP00000367575.2:p.Ile305Leu
ENST00000403558.1:c.1198A>C	ENSP00000384420.1:p.Ile400Leu
ENST00000528996.1:c.270A>C	ENSP00000431226.1:n.270A>C
ENST00000530113.1:n.526A>C
ENST00000531133.5:c.570A>C	ENSP00000435431.1:n.570A>C
ENST00000531797.5:c.*94A>C	ENSP00000432554.1:n.*94A>C
ENST00000619430.1:c.349-149A>C	ENSP00000478572.1:n.349-149A>C
NM_000062.2:c.1069A>C , LRG_105t1:c.1069A>C	NP_000053.2:p.Ile357Leu
NM_001032295.1:c.1069A>C	NP_001027466.1:p.Ile357Leu
NM_000062.3:c.1069A>C MANE Select	NP_000053.2:p.Ile357Leu
NM_001032295.2:c.1069A>C	NP_001027466.1:p.Ile357Leu