Canonical Allele Identifier: CA380698875

Gene: SERPING1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57606067C>G , CM000673.2:g.57606067C>G	GRCh38
NC_000011.9:g.57373540C>G , CM000673.1:g.57373540C>G	GRCh37
NC_000011.8:g.57130116C>G	NCBI36
NG_009625.1:g.13514C>G , LRG_105:g.13514C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000062.3:c.743C>G MANE Select	NP_000053.2:p.Pro248Arg
ENST00000278407.9:c.743C>G MANE Select	ENSP00000278407.4:p.Pro248Arg
NM_000062.2:c.743C>G , LRG_105t1:c.743C>G	NP_000053.2:p.Pro248Arg
NM_001032295.1:c.743C>G	NP_001027466.1:p.Pro248Arg
NM_001032295.2:c.743C>G	NP_001027466.1:p.Pro248Arg
ENST00000278407.8:c.743C>G	ENSP00000278407.4:p.Pro248Arg
ENST00000340687.10:c.743C>G	ENSP00000341861.6:p.Pro248Arg
ENST00000378323.8:c.758C>G	ENSP00000367574.4:p.Pro253Arg
ENST00000378324.6:c.587C>G	ENSP00000367575.2:p.Pro196Arg
ENST00000403558.1:c.845C>G	ENSP00000384420.1:p.Pro282Arg
ENST00000528996.2:c.59-5659C>G	ENSP00000431226.2:n.59-5659C>G
ENST00000531133.5:c.244C>G	ENSP00000435431.1:n.244C>G
ENST00000531605.2:c.*519C>G	ENSP00000503752.1:n.*519C>G
ENST00000531797.5:c.*54+3898C>G	ENSP00000432554.1:n.*54+3898C>G
ENST00000619430.1:c.349-5838C>G	ENSP00000478572.1:n.349-5838C>G
ENST00000619430.2:c.686-341C>G	ENSP00000478572.2:n.686-341C>G
ENST00000676670.1:c.743C>G	ENSP00000504807.1:p.Pro248Arg
ENST00000676741.1:n.1825C>G
ENST00000677624.1:c.*163C>G	ENSP00000503979.1:n.*163C>G
ENST00000677625.1:c.743C>G	ENSP00000502857.1:p.Pro248Arg
ENST00000677856.1:n.802C>G
ENST00000677915.1:c.685+3898C>G	ENSP00000503118.1:n.685+3898C>G
ENST00000678533.1:c.*297C>G	ENSP00000503873.1:n.*297C>G
ENST00000678592.1:c.743C>G	ENSP00000504424.1:p.Pro248Arg