Canonical Allele Identifier: CA380690762

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381960T>C (hg19) ; chr11:g.57614487T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614487T>C , CM000673.2:g.57614487T>C	GRCh38
NC_000011.9:g.57381960T>C , CM000673.1:g.57381960T>C	GRCh37
NC_000011.8:g.57138536T>C	NCBI36
NG_009625.1:g.21934T>C , LRG_105:g.21934T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1409T>C MANE Select	ENSP00000278407.4:p.Val470Ala
ENST00000528996.2:c.*306T>C	ENSP00000431226.2:n.*306T>C
ENST00000531605.2:c.*1185T>C	ENSP00000503752.1:n.*1185T>C
ENST00000619430.2:c.1205T>C	ENSP00000478572.2:p.Val402Ala
ENST00000676670.1:c.1409T>C	ENSP00000504807.1:p.Val470Ala
ENST00000676741.1:n.2491T>C
ENST00000677624.1:c.*829T>C	ENSP00000503979.1:n.*829T>C
ENST00000677625.1:c.1355T>C	ENSP00000502857.1:p.Val452Ala
ENST00000677856.1:n.1662T>C
ENST00000677915.1:c.*306T>C	ENSP00000503118.1:n.*306T>C
ENST00000678533.1:c.*963T>C	ENSP00000503873.1:n.*963T>C
ENST00000678592.1:c.*349T>C	ENSP00000504424.1:n.*349T>C
ENST00000278407.8:c.1409T>C	ENSP00000278407.4:p.Val470Ala
ENST00000340687.10:c.1298T>C	ENSP00000341861.6:p.Val433Ala
ENST00000378323.8:c.1424T>C	ENSP00000367574.4:p.Val475Ala
ENST00000378324.6:c.1253T>C	ENSP00000367575.2:p.Val418Ala
ENST00000403558.1:c.1538T>C	ENSP00000384420.1:p.Val513Ala
ENST00000528996.1:c.610T>C	ENSP00000431226.1:n.610T>C
ENST00000530113.1:n.866T>C
ENST00000531133.5:c.910T>C	ENSP00000435431.1:n.910T>C
ENST00000531797.5:c.*434T>C	ENSP00000432554.1:n.*434T>C
ENST00000619430.1:c.540T>C	ENSP00000478572.1:n.540T>C
NM_000062.2:c.1409T>C , LRG_105t1:c.1409T>C	NP_000053.2:p.Val470Ala
NM_001032295.1:c.1409T>C	NP_001027466.1:p.Val470Ala
NM_000062.3:c.1409T>C MANE Select	NP_000053.2:p.Val470Ala
NM_001032295.2:c.1409T>C	NP_001027466.1:p.Val470Ala