Canonical Allele Identifier: CA380699775

Gene: SERPING1

Linked Data

• gnomAD v4: 11-57606202-T-G
• MyVariant Identifiers: chr11:g.57373675T>G (hg19) ; chr11:g.57606202T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57606202T>G , CM000673.2:g.57606202T>G	GRCh38
NC_000011.9:g.57373675T>G , CM000673.1:g.57373675T>G	GRCh37
NC_000011.8:g.57130251T>G	NCBI36
NG_009625.1:g.13649T>G , LRG_105:g.13649T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.878T>G MANE Select	ENSP00000278407.4:p.Ile293Ser
ENST00000528996.2:c.59-5524T>G	ENSP00000431226.2:n.59-5524T>G
ENST00000531605.2:c.*654T>G	ENSP00000503752.1:n.*654T>G
ENST00000619430.2:c.686-206T>G	ENSP00000478572.2:n.686-206T>G
ENST00000676670.1:c.878T>G	ENSP00000504807.1:p.Ile293Ser
ENST00000676741.1:n.1960T>G
ENST00000677624.1:c.*298T>G	ENSP00000503979.1:n.*298T>G
ENST00000677625.1:c.878T>G	ENSP00000502857.1:p.Ile293Ser
ENST00000677856.1:n.937T>G
ENST00000677915.1:c.685+4033T>G	ENSP00000503118.1:n.685+4033T>G
ENST00000678533.1:c.*432T>G	ENSP00000503873.1:n.*432T>G
ENST00000678592.1:c.878T>G	ENSP00000504424.1:p.Ile293Ser
ENST00000278407.8:c.878T>G	ENSP00000278407.4:p.Ile293Ser
ENST00000340687.10:c.878T>G	ENSP00000341861.6:p.Ile293Ser
ENST00000378323.8:c.893T>G	ENSP00000367574.4:p.Ile298Ser
ENST00000378324.6:c.722T>G	ENSP00000367575.2:p.Ile241Ser
ENST00000403558.1:c.980T>G	ENSP00000384420.1:p.Ile327Ser
ENST00000531133.5:c.379T>G	ENSP00000435431.1:n.379T>G
ENST00000531797.5:c.*54+4033T>G	ENSP00000432554.1:n.*54+4033T>G
ENST00000619430.1:c.349-5703T>G	ENSP00000478572.1:n.349-5703T>G
NM_000062.2:c.878T>G , LRG_105t1:c.878T>G	NP_000053.2:p.Ile293Ser
NM_001032295.1:c.878T>G	NP_001027466.1:p.Ile293Ser
NM_000062.3:c.878T>G MANE Select	NP_000053.2:p.Ile293Ser
NM_001032295.2:c.878T>G	NP_001027466.1:p.Ile293Ser