Canonical Allele Identifier: CA380696914

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57369546C>T (hg19) ; chr11:g.57602073C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57602073C>T , CM000673.2:g.57602073C>T	GRCh38
NC_000011.9:g.57369546C>T , CM000673.1:g.57369546C>T	GRCh37
NC_000011.8:g.57126122C>T	NCBI36
NG_009625.1:g.9520C>T , LRG_105:g.9520C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.589C>T MANE Select	ENSP00000278407.4:p.Leu197Phe
ENST00000528996.2:c.58+3745C>T	ENSP00000431226.2:n.58+3745C>T
ENST00000531605.2:c.90C>T	ENSP00000503752.1:p.Ser30=
ENST00000619430.2:c.589C>T	ENSP00000478572.2:p.Leu197Phe
ENST00000676670.1:c.589C>T	ENSP00000504807.1:p.Leu197Phe
ENST00000676741.1:n.1671C>T
ENST00000677275.1:n.576C>T
ENST00000677624.1:c.589C>T	ENSP00000503979.1:p.Leu197Phe
ENST00000677625.1:c.589C>T	ENSP00000502857.1:p.Leu197Phe
ENST00000677856.1:n.648C>T
ENST00000677915.1:c.589C>T	ENSP00000503118.1:p.Leu197Phe
ENST00000678533.1:c.90C>T	ENSP00000503873.1:p.Ser30=
ENST00000678592.1:c.589C>T	ENSP00000504424.1:p.Leu197Phe
ENST00000278407.8:c.589C>T	ENSP00000278407.4:p.Leu197Phe
ENST00000340687.10:c.589C>T	ENSP00000341861.6:p.Leu197Phe
ENST00000378323.8:c.604C>T	ENSP00000367574.4:p.Leu202Phe
ENST00000378324.6:c.433C>T	ENSP00000367575.2:p.Leu145Phe
ENST00000403558.1:c.691C>T	ENSP00000384420.1:p.Leu231Phe
ENST00000531133.5:c.90C>T	ENSP00000435431.1:p.Ser30=
ENST00000531605.1:n.29C>T
ENST00000531797.5:c.90C>T	ENSP00000432554.1:p.Ser30=
ENST00000619430.1:c.348+1898C>T	ENSP00000478572.1:n.348+1898C>T
NM_000062.2:c.589C>T , LRG_105t1:c.589C>T	NP_000053.2:p.Leu197Phe
NM_001032295.1:c.589C>T	NP_001027466.1:p.Leu197Phe
NM_000062.3:c.589C>T MANE Select	NP_000053.2:p.Leu197Phe
NM_001032295.2:c.589C>T	NP_001027466.1:p.Leu197Phe