Canonical Allele Identifier: CA1975539346

Gene: SERPING1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614553T= , CM000673.2:g.57614553T=	GRCh38
NC_000011.9:g.57382026T= , CM000673.1:g.57382026T=	GRCh37
NC_000011.8:g.57138602T=	NCBI36
NG_009625.1:g.22000T= , LRG_105:g.22000T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000062.3:c.1475T= MANE Select	NP_000053.2:p.Met492=
ENST00000278407.9:c.1475T= MANE Select	ENSP00000278407.4:p.Met492=
NM_000062.2:c.1475T= , LRG_105t1:c.1475T=	NP_000053.2:p.Met492=
NM_001032295.1:c.1475T=	NP_001027466.1:p.Met492=
NM_001032295.2:c.1475T=	NP_001027466.1:p.Met492=
ENST00000278407.8:c.1475T=	ENSP00000278407.4:p.Met492=
ENST00000340687.10:c.1364T=	ENSP00000341861.6:p.Met455=
ENST00000378323.8:c.1490T=	ENSP00000367574.4:p.Met497=
ENST00000378324.6:c.1319T=	ENSP00000367575.2:p.Met440=
ENST00000403558.1:c.1604T=	ENSP00000384420.1:p.Met535=
ENST00000528996.1:c.676T=	ENSP00000431226.1:n.676T=
ENST00000528996.2:c.*372T=	ENSP00000431226.2:n.*372T=
ENST00000531133.5:c.976T=	ENSP00000435431.1:n.976T=
ENST00000531605.2:c.*1251T=	ENSP00000503752.1:n.*1251T=
ENST00000531797.5:c.*500T=	ENSP00000432554.1:n.*500T=
ENST00000619430.1:c.606T=	ENSP00000478572.1:n.606T=
ENST00000619430.2:c.1271T=	ENSP00000478572.2:p.Met424=
ENST00000676670.1:c.1475T=	ENSP00000504807.1:p.Met492=
ENST00000676741.1:n.2557T=
ENST00000677624.1:c.*895T=	ENSP00000503979.1:n.*895T=
ENST00000677625.1:c.1421T=	ENSP00000502857.1:p.Met474=
ENST00000677856.1:n.1728T=
ENST00000677915.1:c.*372T=	ENSP00000503118.1:n.*372T=
ENST00000678533.1:c.*1029T=	ENSP00000503873.1:n.*1029T=
ENST00000678592.1:c.*415T=	ENSP00000504424.1:n.*415T=