Canonical Allele Identifier: CA474806900

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381961C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614488C>T , CM000673.2:g.57614488C>T	GRCh38
NC_000011.9:g.57381961C>T , CM000673.1:g.57381961C>T	GRCh37
NC_000011.8:g.57138537C>T	NCBI36
NG_009625.1:g.21935C>T , LRG_105:g.21935C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1410C>T MANE Select	ENSP00000278407.4:p.Val470=
ENST00000528996.2:c.*307C>T	ENSP00000431226.2:n.*307C>T
ENST00000531605.2:c.*1186C>T	ENSP00000503752.1:n.*1186C>T
ENST00000619430.2:c.1206C>T	ENSP00000478572.2:p.Val402=
ENST00000676670.1:c.1410C>T	ENSP00000504807.1:p.Val470=
ENST00000676741.1:n.2492C>T
ENST00000677624.1:c.*830C>T	ENSP00000503979.1:n.*830C>T
ENST00000677625.1:c.1356C>T	ENSP00000502857.1:p.Val452=
ENST00000677856.1:n.1663C>T
ENST00000677915.1:c.*307C>T	ENSP00000503118.1:n.*307C>T
ENST00000678533.1:c.*964C>T	ENSP00000503873.1:n.*964C>T
ENST00000678592.1:c.*350C>T	ENSP00000504424.1:n.*350C>T
ENST00000278407.8:c.1410C>T	ENSP00000278407.4:p.Val470=
ENST00000340687.10:c.1299C>T	ENSP00000341861.6:p.Val433=
ENST00000378323.8:c.1425C>T	ENSP00000367574.4:p.Val475=
ENST00000378324.6:c.1254C>T	ENSP00000367575.2:p.Val418=
ENST00000403558.1:c.1539C>T	ENSP00000384420.1:p.Val513=
ENST00000528996.1:c.611C>T	ENSP00000431226.1:n.611C>T
ENST00000530113.1:n.867C>T
ENST00000531133.5:c.911C>T	ENSP00000435431.1:n.911C>T
ENST00000531797.5:c.*435C>T	ENSP00000432554.1:n.*435C>T
ENST00000619430.1:c.541C>T	ENSP00000478572.1:n.541C>T
NM_000062.2:c.1410C>T , LRG_105t1:c.1410C>T	NP_000053.2:p.Val470=
NM_001032295.1:c.1410C>T	NP_001027466.1:p.Val470=
NM_000062.3:c.1410C>T MANE Select	NP_000053.2:p.Val470=
NM_001032295.2:c.1410C>T	NP_001027466.1:p.Val470=