Canonical Allele Identifier: CA678581139

Gene: SERPING1

Linked Data

• dbSNP Id: rs1251506361
• MyVariant Identifiers: chr11:g.57382103_57382115del (hg19) ; chr11:g.57614630_57614642del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614632_57614644del , CM000673.2:g.57614632_57614644del	GRCh38
NC_000011.9:g.57382105_57382117del , CM000673.1:g.57382105_57382117del	GRCh37
NC_000011.8:g.57138681_57138693del	NCBI36
NG_009625.1:g.22079_22091del , LRG_105:g.22079_22091del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.*51_*63del MANE Select	ENSP00000278407.4:n.*51_*63del
ENST00000528996.2:c.*451_*463del	ENSP00000431226.2:n.*451_*463del
ENST00000531605.2:c.*1330_*1342del	ENSP00000503752.1:n.*1330_*1342del
ENST00000619430.2:c.*51_*63del	ENSP00000478572.2:n.*51_*63del
ENST00000676670.1:c.*15+36_*15+48del	ENSP00000504807.1:n.*15+36_*15+48del
ENST00000676741.1:n.2636_2648del
ENST00000677624.1:c.*974_*986del	ENSP00000503979.1:n.*974_*986del
ENST00000677625.1:c.*51_*63del	ENSP00000502857.1:n.*51_*63del
ENST00000677856.1:n.1807_1819del
ENST00000677915.1:c.*451_*463del	ENSP00000503118.1:n.*451_*463del
ENST00000678533.1:c.*1072+36_*1072+48del	ENSP00000503873.1:n.*1072+36_*1072+48del
ENST00000678592.1:c.*494_*506del	ENSP00000504424.1:n.*494_*506del
ENST00000278407.8:c.*51_*63del	ENSP00000278407.4:n.*51_*63del
ENST00000340687.10:c.*51_*63del	ENSP00000341861.6:n.*51_*63del
ENST00000378323.8:c.*51_*63del	ENSP00000367574.4:n.*51_*63del
ENST00000378324.6:c.*51_*63del	ENSP00000367575.2:n.*51_*63del
ENST00000403558.1:c.*51_*63del	ENSP00000384420.1:n.*51_*63del
ENST00000528996.1:c.755_767del	ENSP00000431226.1:n.755_767del
ENST00000531797.5:c.*579_*591del	ENSP00000432554.1:n.*579_*591del
NM_000062.2:c.*51_*63del , LRG_105t1:c.*51_*63del	NP_000053.2:n.*51_*63del
NM_001032295.1:c.*51_*63del	NP_001027466.1:n.*51_*63del
NM_000062.3:c.*51_*63del MANE Select	NP_000053.2:n.*51_*63del
NM_001032295.2:c.*51_*63del	NP_001027466.1:n.*51_*63del