Canonical Allele Identifier: CA380702569

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57379242A>C (hg19) ; chr11:g.57611769A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611769A>C , CM000673.2:g.57611769A>C	GRCh38
NC_000011.9:g.57379242A>C , CM000673.1:g.57379242A>C	GRCh37
NC_000011.8:g.57135818A>C	NCBI36
NG_009625.1:g.19216A>C , LRG_105:g.19216A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1082A>C MANE Select	ENSP00000278407.4:p.Gln361Pro
ENST00000528996.2:c.102A>C	ENSP00000431226.2:p.Pro34=
ENST00000531605.2:c.*858A>C	ENSP00000503752.1:n.*858A>C
ENST00000619430.2:c.878A>C	ENSP00000478572.2:p.Gln293Pro
ENST00000676670.1:c.1082A>C	ENSP00000504807.1:p.Gln361Pro
ENST00000676741.1:n.2164A>C
ENST00000677624.1:c.*502A>C	ENSP00000503979.1:n.*502A>C
ENST00000677625.1:c.1030-2A>C	ENSP00000502857.1:n.1030-2A>C
ENST00000677856.1:n.1335A>C
ENST00000677915.1:c.738A>C	ENSP00000503118.1:p.Pro246=
ENST00000678533.1:c.*636A>C	ENSP00000503873.1:n.*636A>C
ENST00000678592.1:c.*22A>C	ENSP00000504424.1:n.*22A>C
ENST00000278407.8:c.1082A>C	ENSP00000278407.4:p.Gln361Pro
ENST00000340687.10:c.1030-59A>C	ENSP00000341861.6:n.1030-59A>C
ENST00000378323.8:c.1097A>C	ENSP00000367574.4:p.Gln366Pro
ENST00000378324.6:c.926A>C	ENSP00000367575.2:p.Gln309Pro
ENST00000403558.1:c.1211A>C	ENSP00000384420.1:p.Gln404Pro
ENST00000528996.1:c.283A>C	ENSP00000431226.1:n.283A>C
ENST00000530113.1:n.539A>C
ENST00000531133.5:c.583A>C	ENSP00000435431.1:n.583A>C
ENST00000531797.5:c.*107A>C	ENSP00000432554.1:n.*107A>C
ENST00000619430.1:c.349-136A>C	ENSP00000478572.1:n.349-136A>C
NM_000062.2:c.1082A>C , LRG_105t1:c.1082A>C	NP_000053.2:p.Gln361Pro
NM_001032295.1:c.1082A>C	NP_001027466.1:p.Gln361Pro
NM_000062.3:c.1082A>C MANE Select	NP_000053.2:p.Gln361Pro
NM_001032295.2:c.1082A>C	NP_001027466.1:p.Gln361Pro