Canonical Allele Identifier: CA380690696

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381923G>T (hg19) ; chr11:g.57614450G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614450G>T , CM000673.2:g.57614450G>T	GRCh38
NC_000011.9:g.57381923G>T , CM000673.1:g.57381923G>T	GRCh37
NC_000011.8:g.57138499G>T	NCBI36
NG_009625.1:g.21897G>T , LRG_105:g.21897G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1372G>T MANE Select	ENSP00000278407.4:p.Ala458Ser
ENST00000528996.2:c.*269G>T	ENSP00000431226.2:n.*269G>T
ENST00000531605.2:c.*1148G>T	ENSP00000503752.1:n.*1148G>T
ENST00000619430.2:c.1168G>T	ENSP00000478572.2:p.Ala390Ser
ENST00000676670.1:c.1372G>T	ENSP00000504807.1:p.Ala458Ser
ENST00000676741.1:n.2454G>T
ENST00000677624.1:c.*792G>T	ENSP00000503979.1:n.*792G>T
ENST00000677625.1:c.1318G>T	ENSP00000502857.1:p.Ala440Ser
ENST00000677856.1:n.1625G>T
ENST00000677915.1:c.*269G>T	ENSP00000503118.1:n.*269G>T
ENST00000678533.1:c.*926G>T	ENSP00000503873.1:n.*926G>T
ENST00000678592.1:c.*312G>T	ENSP00000504424.1:n.*312G>T
ENST00000278407.8:c.1372G>T	ENSP00000278407.4:p.Ala458Ser
ENST00000340687.10:c.1261G>T	ENSP00000341861.6:p.Ala421Ser
ENST00000378323.8:c.1387G>T	ENSP00000367574.4:p.Ala463Ser
ENST00000378324.6:c.1216G>T	ENSP00000367575.2:p.Ala406Ser
ENST00000403558.1:c.1501G>T	ENSP00000384420.1:p.Ala501Ser
ENST00000528996.1:c.573G>T	ENSP00000431226.1:n.573G>T
ENST00000530113.1:n.829G>T
ENST00000531133.5:c.873G>T	ENSP00000435431.1:n.873G>T
ENST00000531797.5:c.*397G>T	ENSP00000432554.1:n.*397G>T
ENST00000619430.1:c.503G>T	ENSP00000478572.1:n.503G>T
NM_000062.2:c.1372G>T , LRG_105t1:c.1372G>T	NP_000053.2:p.Ala458Ser
NM_001032295.1:c.1372G>T	NP_001027466.1:p.Ala458Ser
NM_000062.3:c.1372G>T MANE Select	NP_000053.2:p.Ala458Ser
NM_001032295.2:c.1372G>T	NP_001027466.1:p.Ala458Ser