Canonical Allele Identifier: CA380690820

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381986T>C (hg19) ; chr11:g.57614513T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614513T>C , CM000673.2:g.57614513T>C	GRCh38
NC_000011.9:g.57381986T>C , CM000673.1:g.57381986T>C	GRCh37
NC_000011.8:g.57138562T>C	NCBI36
NG_009625.1:g.21960T>C , LRG_105:g.21960T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1435T>C MANE Select	ENSP00000278407.4:p.Phe479Leu
ENST00000528996.2:c.*332T>C	ENSP00000431226.2:n.*332T>C
ENST00000531605.2:c.*1211T>C	ENSP00000503752.1:n.*1211T>C
ENST00000619430.2:c.1231T>C	ENSP00000478572.2:p.Phe411Leu
ENST00000676670.1:c.1435T>C	ENSP00000504807.1:p.Phe479Leu
ENST00000676741.1:n.2517T>C
ENST00000677624.1:c.*855T>C	ENSP00000503979.1:n.*855T>C
ENST00000677625.1:c.1381T>C	ENSP00000502857.1:p.Phe461Leu
ENST00000677856.1:n.1688T>C
ENST00000677915.1:c.*332T>C	ENSP00000503118.1:n.*332T>C
ENST00000678533.1:c.*989T>C	ENSP00000503873.1:n.*989T>C
ENST00000678592.1:c.*375T>C	ENSP00000504424.1:n.*375T>C
ENST00000278407.8:c.1435T>C	ENSP00000278407.4:p.Phe479Leu
ENST00000340687.10:c.1324T>C	ENSP00000341861.6:p.Phe442Leu
ENST00000378323.8:c.1450T>C	ENSP00000367574.4:p.Phe484Leu
ENST00000378324.6:c.1279T>C	ENSP00000367575.2:p.Phe427Leu
ENST00000403558.1:c.1564T>C	ENSP00000384420.1:p.Phe522Leu
ENST00000528996.1:c.636T>C	ENSP00000431226.1:n.636T>C
ENST00000530113.1:n.892T>C
ENST00000531133.5:c.936T>C	ENSP00000435431.1:n.936T>C
ENST00000531797.5:c.*460T>C	ENSP00000432554.1:n.*460T>C
ENST00000619430.1:c.566T>C	ENSP00000478572.1:n.566T>C
NM_000062.2:c.1435T>C , LRG_105t1:c.1435T>C	NP_000053.2:p.Phe479Leu
NM_001032295.1:c.1435T>C	NP_001027466.1:p.Phe479Leu
NM_000062.3:c.1435T>C MANE Select	NP_000053.2:p.Phe479Leu
NM_001032295.2:c.1435T>C	NP_001027466.1:p.Phe479Leu