Canonical Allele Identifier: CA380703155

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57379330G>T (hg19) ; chr11:g.57611857G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611857G>T , CM000673.2:g.57611857G>T	GRCh38
NC_000011.9:g.57379330G>T , CM000673.1:g.57379330G>T	GRCh37
NC_000011.8:g.57135906G>T	NCBI36
NG_009625.1:g.19304G>T , LRG_105:g.19304G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1170G>T MANE Select	ENSP00000278407.4:p.Lys390Asn
ENST00000528996.2:c.*67G>T	ENSP00000431226.2:n.*67G>T
ENST00000531605.2:c.*946G>T	ENSP00000503752.1:n.*946G>T
ENST00000619430.2:c.966G>T	ENSP00000478572.2:p.Lys322Asn
ENST00000676670.1:c.1170G>T	ENSP00000504807.1:p.Lys390Asn
ENST00000676741.1:n.2252G>T
ENST00000677624.1:c.*590G>T	ENSP00000503979.1:n.*590G>T
ENST00000677625.1:c.1116G>T	ENSP00000502857.1:p.Lys372Asn
ENST00000677856.1:n.1423G>T
ENST00000677915.1:c.*67G>T	ENSP00000503118.1:n.*67G>T
ENST00000678533.1:c.*724G>T	ENSP00000503873.1:n.*724G>T
ENST00000678592.1:c.*110G>T	ENSP00000504424.1:n.*110G>T
ENST00000278407.8:c.1170G>T	ENSP00000278407.4:p.Lys390Asn
ENST00000340687.10:c.1059G>T	ENSP00000341861.6:p.Lys353Asn
ENST00000378323.8:c.1185G>T	ENSP00000367574.4:p.Lys395Asn
ENST00000378324.6:c.1014G>T	ENSP00000367575.2:p.Lys338Asn
ENST00000403558.1:c.1299G>T	ENSP00000384420.1:p.Lys433Asn
ENST00000528996.1:c.371G>T	ENSP00000431226.1:n.371G>T
ENST00000530113.1:n.627G>T
ENST00000531133.5:c.671G>T	ENSP00000435431.1:n.671G>T
ENST00000531797.5:c.*195G>T	ENSP00000432554.1:n.*195G>T
ENST00000619430.1:c.349-48G>T	ENSP00000478572.1:n.349-48G>T
NM_000062.2:c.1170G>T , LRG_105t1:c.1170G>T	NP_000053.2:p.Lys390Asn
NM_001032295.1:c.1170G>T	NP_001027466.1:p.Lys390Asn
NM_000062.3:c.1170G>T MANE Select	NP_000053.2:p.Lys390Asn
NM_001032295.2:c.1170G>T	NP_001027466.1:p.Lys390Asn