Canonical Allele Identifier: CA380702596

Gene: SERPING1

Linked Data

• gnomAD v4: 11-57611772-A-C
• MyVariant Identifiers: chr11:g.57379245A>C (hg19) ; chr11:g.57611772A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611772A>C , CM000673.2:g.57611772A>C	GRCh38
NC_000011.9:g.57379245A>C , CM000673.1:g.57379245A>C	GRCh37
NC_000011.8:g.57135821A>C	NCBI36
NG_009625.1:g.19219A>C , LRG_105:g.19219A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1085A>C MANE Select	ENSP00000278407.4:p.Asn362Thr
ENST00000528996.2:c.105A>C	ENSP00000431226.2:p.Glu35Asp
ENST00000531605.2:c.*861A>C	ENSP00000503752.1:n.*861A>C
ENST00000619430.2:c.881A>C	ENSP00000478572.2:p.Asn294Thr
ENST00000676670.1:c.1085A>C	ENSP00000504807.1:p.Asn362Thr
ENST00000676741.1:n.2167A>C
ENST00000677624.1:c.*505A>C	ENSP00000503979.1:n.*505A>C
ENST00000677625.1:c.1031A>C	ENSP00000502857.1:p.Asn344Thr
ENST00000677856.1:n.1338A>C
ENST00000677915.1:c.741A>C	ENSP00000503118.1:p.Glu247Asp
ENST00000678533.1:c.*639A>C	ENSP00000503873.1:n.*639A>C
ENST00000678592.1:c.*25A>C	ENSP00000504424.1:n.*25A>C
ENST00000278407.8:c.1085A>C	ENSP00000278407.4:p.Asn362Thr
ENST00000340687.10:c.1030-56A>C	ENSP00000341861.6:n.1030-56A>C
ENST00000378323.8:c.1100A>C	ENSP00000367574.4:p.Asn367Thr
ENST00000378324.6:c.929A>C	ENSP00000367575.2:p.Asn310Thr
ENST00000403558.1:c.1214A>C	ENSP00000384420.1:p.Asn405Thr
ENST00000528996.1:c.286A>C	ENSP00000431226.1:n.286A>C
ENST00000530113.1:n.542A>C
ENST00000531133.5:c.586A>C	ENSP00000435431.1:n.586A>C
ENST00000531797.5:c.*110A>C	ENSP00000432554.1:n.*110A>C
ENST00000619430.1:c.349-133A>C	ENSP00000478572.1:n.349-133A>C
NM_000062.2:c.1085A>C , LRG_105t1:c.1085A>C	NP_000053.2:p.Asn362Thr
NM_001032295.1:c.1085A>C	NP_001027466.1:p.Asn362Thr
NM_000062.3:c.1085A>C MANE Select	NP_000053.2:p.Asn362Thr
NM_001032295.2:c.1085A>C	NP_001027466.1:p.Asn362Thr