Canonical Allele Identifier: CA2975130767

Gene: SERPING1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614502_57614504del , CM000673.2:g.57614502_57614504del	GRCh38
NC_000011.9:g.57381975_57381977del , CM000673.1:g.57381975_57381977del	GRCh37
NC_000011.8:g.57138551_57138553del	NCBI36
NG_009625.1:g.21949_21951del , LRG_105:g.21949_21951del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1424_1426del MANE Select	ENSP00000278407.4:p.Gln475del
ENST00000528996.2:c.*321_*323del	ENSP00000431226.2:n.*321_*323del
ENST00000531605.2:c.*1200_*1202del	ENSP00000503752.1:n.*1200_*1202del
ENST00000619430.2:c.1220_1222del	ENSP00000478572.2:p.Gln407del
ENST00000676670.1:c.1424_1426del	ENSP00000504807.1:p.Gln475del
ENST00000676741.1:n.2506_2508del
ENST00000677624.1:c.*844_*846del	ENSP00000503979.1:n.*844_*846del
ENST00000677625.1:c.1370_1372del	ENSP00000502857.1:p.Gln457del
ENST00000677856.1:n.1677_1679del
ENST00000677915.1:c.*321_*323del	ENSP00000503118.1:n.*321_*323del
ENST00000678533.1:c.*978_*980del	ENSP00000503873.1:n.*978_*980del
ENST00000678592.1:c.*364_*366del	ENSP00000504424.1:n.*364_*366del
ENST00000278407.8:c.1424_1426del	ENSP00000278407.4:p.Gln475del
ENST00000340687.10:c.1313_1315del	ENSP00000341861.6:p.Gln438del
ENST00000378323.8:c.1439_1441del	ENSP00000367574.4:p.Gln480del
ENST00000378324.6:c.1268_1270del	ENSP00000367575.2:p.Gln423del
ENST00000403558.1:c.1553_1555del	ENSP00000384420.1:p.Gln518del
ENST00000528996.1:c.625_627del	ENSP00000431226.1:n.625_627del
ENST00000530113.1:n.881_883del
ENST00000531133.5:c.925_927del	ENSP00000435431.1:n.925_927del
ENST00000531797.5:c.*449_*451del	ENSP00000432554.1:n.*449_*451del
ENST00000619430.1:c.555_557del	ENSP00000478572.1:n.555_557del
NM_000062.2:c.1424_1426del , LRG_105t1:c.1424_1426del	NP_000053.2:p.Gln475del
NM_001032295.1:c.1424_1426del	NP_001027466.1:p.Gln475del
NM_000062.3:c.1424_1426del MANE Select	NP_000053.2:p.Gln475del
NM_001032295.2:c.1424_1426del	NP_001027466.1:p.Gln475del