Canonical Allele Identifier: CA380703210

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57379337C>T (hg19) ; chr11:g.57611864C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611864C>T , CM000673.2:g.57611864C>T	GRCh38
NC_000011.9:g.57379337C>T , CM000673.1:g.57379337C>T	GRCh37
NC_000011.8:g.57135913C>T	NCBI36
NG_009625.1:g.19311C>T , LRG_105:g.19311C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1177C>T MANE Select	ENSP00000278407.4:p.Pro393Ser
ENST00000528996.2:c.*74C>T	ENSP00000431226.2:n.*74C>T
ENST00000531605.2:c.*953C>T	ENSP00000503752.1:n.*953C>T
ENST00000619430.2:c.973C>T	ENSP00000478572.2:p.Pro325Ser
ENST00000676670.1:c.1177C>T	ENSP00000504807.1:p.Pro393Ser
ENST00000676741.1:n.2259C>T
ENST00000677624.1:c.*597C>T	ENSP00000503979.1:n.*597C>T
ENST00000677625.1:c.1123C>T	ENSP00000502857.1:p.Pro375Ser
ENST00000677856.1:n.1430C>T
ENST00000677915.1:c.*74C>T	ENSP00000503118.1:n.*74C>T
ENST00000678533.1:c.*731C>T	ENSP00000503873.1:n.*731C>T
ENST00000678592.1:c.*117C>T	ENSP00000504424.1:n.*117C>T
ENST00000278407.8:c.1177C>T	ENSP00000278407.4:p.Pro393Ser
ENST00000340687.10:c.1066C>T	ENSP00000341861.6:p.Pro356Ser
ENST00000378323.8:c.1192C>T	ENSP00000367574.4:p.Pro398Ser
ENST00000378324.6:c.1021C>T	ENSP00000367575.2:p.Pro341Ser
ENST00000403558.1:c.1306C>T	ENSP00000384420.1:p.Pro436Ser
ENST00000528996.1:c.378C>T	ENSP00000431226.1:n.378C>T
ENST00000530113.1:n.634C>T
ENST00000531133.5:c.678C>T	ENSP00000435431.1:n.678C>T
ENST00000531797.5:c.*202C>T	ENSP00000432554.1:n.*202C>T
ENST00000619430.1:c.349-41C>T	ENSP00000478572.1:n.349-41C>T
NM_000062.2:c.1177C>T , LRG_105t1:c.1177C>T	NP_000053.2:p.Pro393Ser
NM_001032295.1:c.1177C>T	NP_001027466.1:p.Pro393Ser
NM_000062.3:c.1177C>T MANE Select	NP_000053.2:p.Pro393Ser
NM_001032295.2:c.1177C>T	NP_001027466.1:p.Pro393Ser