Canonical Allele Identifier: CA380698765

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57373528A>C (hg19) ; chr11:g.57606055A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57606055A>C , CM000673.2:g.57606055A>C	GRCh38
NC_000011.9:g.57373528A>C , CM000673.1:g.57373528A>C	GRCh37
NC_000011.8:g.57130104A>C	NCBI36
NG_009625.1:g.13502A>C , LRG_105:g.13502A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.731A>C MANE Select	ENSP00000278407.4:p.Tyr244Ser
ENST00000528996.2:c.59-5671A>C	ENSP00000431226.2:n.59-5671A>C
ENST00000531605.2:c.*507A>C	ENSP00000503752.1:n.*507A>C
ENST00000619430.2:c.686-353A>C	ENSP00000478572.2:n.686-353A>C
ENST00000676670.1:c.731A>C	ENSP00000504807.1:p.Tyr244Ser
ENST00000676741.1:n.1813A>C
ENST00000677624.1:c.*151A>C	ENSP00000503979.1:n.*151A>C
ENST00000677625.1:c.731A>C	ENSP00000502857.1:p.Tyr244Ser
ENST00000677856.1:n.790A>C
ENST00000677915.1:c.685+3886A>C	ENSP00000503118.1:n.685+3886A>C
ENST00000678533.1:c.*285A>C	ENSP00000503873.1:n.*285A>C
ENST00000678592.1:c.731A>C	ENSP00000504424.1:p.Tyr244Ser
ENST00000278407.8:c.731A>C	ENSP00000278407.4:p.Tyr244Ser
ENST00000340687.10:c.731A>C	ENSP00000341861.6:p.Tyr244Ser
ENST00000378323.8:c.746A>C	ENSP00000367574.4:p.Tyr249Ser
ENST00000378324.6:c.575A>C	ENSP00000367575.2:p.Tyr192Ser
ENST00000403558.1:c.833A>C	ENSP00000384420.1:p.Tyr278Ser
ENST00000531133.5:c.232A>C	ENSP00000435431.1:n.232A>C
ENST00000531605.1:n.578A>C
ENST00000531797.5:c.*54+3886A>C	ENSP00000432554.1:n.*54+3886A>C
ENST00000619430.1:c.349-5850A>C	ENSP00000478572.1:n.349-5850A>C
NM_000062.2:c.731A>C , LRG_105t1:c.731A>C	NP_000053.2:p.Tyr244Ser
NM_001032295.1:c.731A>C	NP_001027466.1:p.Tyr244Ser
NM_000062.3:c.731A>C MANE Select	NP_000053.2:p.Tyr244Ser
NM_001032295.2:c.731A>C	NP_001027466.1:p.Tyr244Ser