Canonical Allele Identifier: CA380702808

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57379275A>T (hg19) ; chr11:g.57611802A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611802A>T , CM000673.2:g.57611802A>T	GRCh38
NC_000011.9:g.57379275A>T , CM000673.1:g.57379275A>T	GRCh37
NC_000011.8:g.57135851A>T	NCBI36
NG_009625.1:g.19249A>T , LRG_105:g.19249A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1115A>T MANE Select	ENSP00000278407.4:p.Gln372Leu
ENST00000528996.2:c.*12A>T	ENSP00000431226.2:n.*12A>T
ENST00000531605.2:c.*891A>T	ENSP00000503752.1:n.*891A>T
ENST00000619430.2:c.911A>T	ENSP00000478572.2:p.Gln304Leu
ENST00000676670.1:c.1115A>T	ENSP00000504807.1:p.Gln372Leu
ENST00000676741.1:n.2197A>T
ENST00000677624.1:c.*535A>T	ENSP00000503979.1:n.*535A>T
ENST00000677625.1:c.1061A>T	ENSP00000502857.1:p.Gln354Leu
ENST00000677856.1:n.1368A>T
ENST00000677915.1:c.*12A>T	ENSP00000503118.1:n.*12A>T
ENST00000678533.1:c.*669A>T	ENSP00000503873.1:n.*669A>T
ENST00000678592.1:c.*55A>T	ENSP00000504424.1:n.*55A>T
ENST00000278407.8:c.1115A>T	ENSP00000278407.4:p.Gln372Leu
ENST00000340687.10:c.1030-26A>T	ENSP00000341861.6:n.1030-26A>T
ENST00000378323.8:c.1130A>T	ENSP00000367574.4:p.Gln377Leu
ENST00000378324.6:c.959A>T	ENSP00000367575.2:p.Gln320Leu
ENST00000403558.1:c.1244A>T	ENSP00000384420.1:p.Gln415Leu
ENST00000528996.1:c.316A>T	ENSP00000431226.1:n.316A>T
ENST00000530113.1:n.572A>T
ENST00000531133.5:c.616A>T	ENSP00000435431.1:n.616A>T
ENST00000531797.5:c.*140A>T	ENSP00000432554.1:n.*140A>T
ENST00000619430.1:c.349-103A>T	ENSP00000478572.1:n.349-103A>T
NM_000062.2:c.1115A>T , LRG_105t1:c.1115A>T	NP_000053.2:p.Gln372Leu
NM_001032295.1:c.1115A>T	NP_001027466.1:p.Gln372Leu
NM_000062.3:c.1115A>T MANE Select	NP_000053.2:p.Gln372Leu
NM_001032295.2:c.1115A>T	NP_001027466.1:p.Gln372Leu