Canonical Allele Identifier: CA380690783

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381969T>C (hg19) ; chr11:g.57614496T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614496T>C , CM000673.2:g.57614496T>C	GRCh38
NC_000011.9:g.57381969T>C , CM000673.1:g.57381969T>C	GRCh37
NC_000011.8:g.57138545T>C	NCBI36
NG_009625.1:g.21943T>C , LRG_105:g.21943T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1418T>C MANE Select	ENSP00000278407.4:p.Val473Ala
ENST00000528996.2:c.*315T>C	ENSP00000431226.2:n.*315T>C
ENST00000531605.2:c.*1194T>C	ENSP00000503752.1:n.*1194T>C
ENST00000619430.2:c.1214T>C	ENSP00000478572.2:p.Val405Ala
ENST00000676670.1:c.1418T>C	ENSP00000504807.1:p.Val473Ala
ENST00000676741.1:n.2500T>C
ENST00000677624.1:c.*838T>C	ENSP00000503979.1:n.*838T>C
ENST00000677625.1:c.1364T>C	ENSP00000502857.1:p.Val455Ala
ENST00000677856.1:n.1671T>C
ENST00000677915.1:c.*315T>C	ENSP00000503118.1:n.*315T>C
ENST00000678533.1:c.*972T>C	ENSP00000503873.1:n.*972T>C
ENST00000678592.1:c.*358T>C	ENSP00000504424.1:n.*358T>C
ENST00000278407.8:c.1418T>C	ENSP00000278407.4:p.Val473Ala
ENST00000340687.10:c.1307T>C	ENSP00000341861.6:p.Val436Ala
ENST00000378323.8:c.1433T>C	ENSP00000367574.4:p.Val478Ala
ENST00000378324.6:c.1262T>C	ENSP00000367575.2:p.Val421Ala
ENST00000403558.1:c.1547T>C	ENSP00000384420.1:p.Val516Ala
ENST00000528996.1:c.619T>C	ENSP00000431226.1:n.619T>C
ENST00000530113.1:n.875T>C
ENST00000531133.5:c.919T>C	ENSP00000435431.1:n.919T>C
ENST00000531797.5:c.*443T>C	ENSP00000432554.1:n.*443T>C
ENST00000619430.1:c.549T>C	ENSP00000478572.1:n.549T>C
NM_000062.2:c.1418T>C , LRG_105t1:c.1418T>C	NP_000053.2:p.Val473Ala
NM_001032295.1:c.1418T>C	NP_001027466.1:p.Val473Ala
NM_000062.3:c.1418T>C MANE Select	NP_000053.2:p.Val473Ala
NM_001032295.2:c.1418T>C	NP_001027466.1:p.Val473Ala