Canonical Allele Identifier: CA380698513

Gene: SERPING1

Linked Data

• gnomAD v4: 11-57606015-G-T
• MyVariant Identifiers: chr11:g.57373488G>T (hg19) ; chr11:g.57606015G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57606015G>T , CM000673.2:g.57606015G>T	GRCh38
NC_000011.9:g.57373488G>T , CM000673.1:g.57373488G>T	GRCh37
NC_000011.8:g.57130064G>T	NCBI36
NG_009625.1:g.13462G>T , LRG_105:g.13462G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.691G>T MANE Select	ENSP00000278407.4:p.Ala231Ser
ENST00000528996.2:c.59-5711G>T	ENSP00000431226.2:n.59-5711G>T
ENST00000531605.2:c.*467G>T	ENSP00000503752.1:n.*467G>T
ENST00000619430.2:c.686-393G>T	ENSP00000478572.2:n.686-393G>T
ENST00000676670.1:c.691G>T	ENSP00000504807.1:p.Ala231Ser
ENST00000676741.1:n.1773G>T
ENST00000677624.1:c.*111G>T	ENSP00000503979.1:n.*111G>T
ENST00000677625.1:c.691G>T	ENSP00000502857.1:p.Ala231Ser
ENST00000677856.1:n.750G>T
ENST00000677915.1:c.685+3846G>T	ENSP00000503118.1:n.685+3846G>T
ENST00000678533.1:c.*245G>T	ENSP00000503873.1:n.*245G>T
ENST00000678592.1:c.691G>T	ENSP00000504424.1:p.Ala231Ser
ENST00000278407.8:c.691G>T	ENSP00000278407.4:p.Ala231Ser
ENST00000340687.10:c.691G>T	ENSP00000341861.6:p.Ala231Ser
ENST00000378323.8:c.706G>T	ENSP00000367574.4:p.Ala236Ser
ENST00000378324.6:c.535G>T	ENSP00000367575.2:p.Ala179Ser
ENST00000403558.1:c.793G>T	ENSP00000384420.1:p.Ala265Ser
ENST00000531133.5:c.192G>T	ENSP00000435431.1:n.192G>T
ENST00000531605.1:n.538G>T
ENST00000531797.5:c.*54+3846G>T	ENSP00000432554.1:n.*54+3846G>T
ENST00000619430.1:c.348+5840G>T	ENSP00000478572.1:n.348+5840G>T
NM_000062.2:c.691G>T , LRG_105t1:c.691G>T	NP_000053.2:p.Ala231Ser
NM_001032295.1:c.691G>T	NP_001027466.1:p.Ala231Ser
NM_000062.3:c.691G>T MANE Select	NP_000053.2:p.Ala231Ser
NM_001032295.2:c.691G>T	NP_001027466.1:p.Ala231Ser