Canonical Allele Identifier: CA380702749

Gene: SERPING1

Linked Data

• gnomAD v4: 11-57611795-A-G
• MyVariant Identifiers: chr11:g.57379268A>G (hg19) ; chr11:g.57611795A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611795A>G , CM000673.2:g.57611795A>G	GRCh38
NC_000011.9:g.57379268A>G , CM000673.1:g.57379268A>G	GRCh37
NC_000011.8:g.57135844A>G	NCBI36
NG_009625.1:g.19242A>G , LRG_105:g.19242A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1108A>G MANE Select	ENSP00000278407.4:p.Met370Val
ENST00000528996.2:c.*5A>G	ENSP00000431226.2:n.*5A>G
ENST00000531605.2:c.*884A>G	ENSP00000503752.1:n.*884A>G
ENST00000619430.2:c.904A>G	ENSP00000478572.2:p.Met302Val
ENST00000676670.1:c.1108A>G	ENSP00000504807.1:p.Met370Val
ENST00000676741.1:n.2190A>G
ENST00000677624.1:c.*528A>G	ENSP00000503979.1:n.*528A>G
ENST00000677625.1:c.1054A>G	ENSP00000502857.1:p.Met352Val
ENST00000677856.1:n.1361A>G
ENST00000677915.1:c.*5A>G	ENSP00000503118.1:n.*5A>G
ENST00000678533.1:c.*662A>G	ENSP00000503873.1:n.*662A>G
ENST00000678592.1:c.*48A>G	ENSP00000504424.1:n.*48A>G
ENST00000278407.8:c.1108A>G	ENSP00000278407.4:p.Met370Val
ENST00000340687.10:c.1030-33A>G	ENSP00000341861.6:n.1030-33A>G
ENST00000378323.8:c.1123A>G	ENSP00000367574.4:p.Met375Val
ENST00000378324.6:c.952A>G	ENSP00000367575.2:p.Met318Val
ENST00000403558.1:c.1237A>G	ENSP00000384420.1:p.Met413Val
ENST00000528996.1:c.309A>G	ENSP00000431226.1:n.309A>G
ENST00000530113.1:n.565A>G
ENST00000531133.5:c.609A>G	ENSP00000435431.1:n.609A>G
ENST00000531797.5:c.*133A>G	ENSP00000432554.1:n.*133A>G
ENST00000619430.1:c.349-110A>G	ENSP00000478572.1:n.349-110A>G
NM_000062.2:c.1108A>G , LRG_105t1:c.1108A>G	NP_000053.2:p.Met370Val
NM_001032295.1:c.1108A>G	NP_001027466.1:p.Met370Val
NM_000062.3:c.1108A>G MANE Select	NP_000053.2:p.Met370Val
NM_001032295.2:c.1108A>G	NP_001027466.1:p.Met370Val