Canonical Allele Identifier: CA380699821

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57373684G>C (hg19) ; chr11:g.57606211G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57606211G>C , CM000673.2:g.57606211G>C	GRCh38
NC_000011.9:g.57373684G>C , CM000673.1:g.57373684G>C	GRCh37
NC_000011.8:g.57130260G>C	NCBI36
NG_009625.1:g.13658G>C , LRG_105:g.13658G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.887G>C MANE Select	ENSP00000278407.4:p.Ser296Thr
ENST00000528996.2:c.59-5515G>C	ENSP00000431226.2:n.59-5515G>C
ENST00000531605.2:c.*663G>C	ENSP00000503752.1:n.*663G>C
ENST00000619430.2:c.686-197G>C	ENSP00000478572.2:n.686-197G>C
ENST00000676670.1:c.887G>C	ENSP00000504807.1:p.Ser296Thr
ENST00000676741.1:n.1969G>C
ENST00000677624.1:c.*307G>C	ENSP00000503979.1:n.*307G>C
ENST00000677625.1:c.887G>C	ENSP00000502857.1:p.Ser296Thr
ENST00000677856.1:n.946G>C
ENST00000677915.1:c.685+4042G>C	ENSP00000503118.1:n.685+4042G>C
ENST00000678533.1:c.*441G>C	ENSP00000503873.1:n.*441G>C
ENST00000678592.1:c.887G>C	ENSP00000504424.1:p.Ser296Thr
ENST00000278407.8:c.887G>C	ENSP00000278407.4:p.Ser296Thr
ENST00000340687.10:c.887G>C	ENSP00000341861.6:p.Ser296Thr
ENST00000378323.8:c.902G>C	ENSP00000367574.4:p.Ser301Thr
ENST00000378324.6:c.731G>C	ENSP00000367575.2:p.Ser244Thr
ENST00000403558.1:c.989G>C	ENSP00000384420.1:p.Ser330Thr
ENST00000531133.5:c.388G>C	ENSP00000435431.1:n.388G>C
ENST00000531797.5:c.*54+4042G>C	ENSP00000432554.1:n.*54+4042G>C
ENST00000619430.1:c.349-5694G>C	ENSP00000478572.1:n.349-5694G>C
NM_000062.2:c.887G>C , LRG_105t1:c.887G>C	NP_000053.2:p.Ser296Thr
NM_001032295.1:c.887G>C	NP_001027466.1:p.Ser296Thr
NM_000062.3:c.887G>C MANE Select	NP_000053.2:p.Ser296Thr
NM_001032295.2:c.887G>C	NP_001027466.1:p.Ser296Thr