Canonical Allele Identifier: CA380702901

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57379299A>T (hg19) ; chr11:g.57611826A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611826A>T , CM000673.2:g.57611826A>T	GRCh38
NC_000011.9:g.57379299A>T , CM000673.1:g.57379299A>T	GRCh37
NC_000011.8:g.57135875A>T	NCBI36
NG_009625.1:g.19273A>T , LRG_105:g.19273A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1139A>T MANE Select	ENSP00000278407.4:p.Lys380Met
ENST00000528996.2:c.*36A>T	ENSP00000431226.2:n.*36A>T
ENST00000531605.2:c.*915A>T	ENSP00000503752.1:n.*915A>T
ENST00000619430.2:c.935A>T	ENSP00000478572.2:p.Lys312Met
ENST00000676670.1:c.1139A>T	ENSP00000504807.1:p.Lys380Met
ENST00000676741.1:n.2221A>T
ENST00000677624.1:c.*559A>T	ENSP00000503979.1:n.*559A>T
ENST00000677625.1:c.1085A>T	ENSP00000502857.1:p.Lys362Met
ENST00000677856.1:n.1392A>T
ENST00000677915.1:c.*36A>T	ENSP00000503118.1:n.*36A>T
ENST00000678533.1:c.*693A>T	ENSP00000503873.1:n.*693A>T
ENST00000678592.1:c.*79A>T	ENSP00000504424.1:n.*79A>T
ENST00000278407.8:c.1139A>T	ENSP00000278407.4:p.Lys380Met
ENST00000340687.10:c.1030-2A>T	ENSP00000341861.6:n.1030-2A>T
ENST00000378323.8:c.1154A>T	ENSP00000367574.4:p.Lys385Met
ENST00000378324.6:c.983A>T	ENSP00000367575.2:p.Lys328Met
ENST00000403558.1:c.1268A>T	ENSP00000384420.1:p.Lys423Met
ENST00000528996.1:c.340A>T	ENSP00000431226.1:n.340A>T
ENST00000530113.1:n.596A>T
ENST00000531133.5:c.640A>T	ENSP00000435431.1:n.640A>T
ENST00000531797.5:c.*164A>T	ENSP00000432554.1:n.*164A>T
ENST00000619430.1:c.349-79A>T	ENSP00000478572.1:n.349-79A>T
NM_000062.2:c.1139A>T , LRG_105t1:c.1139A>T	NP_000053.2:p.Lys380Met
NM_001032295.1:c.1139A>T	NP_001027466.1:p.Lys380Met
NM_000062.3:c.1139A>T MANE Select	NP_000053.2:p.Lys380Met
NM_001032295.2:c.1139A>T	NP_001027466.1:p.Lys380Met