Canonical Allele Identifier: CA6008235

Gene: SERPING1

Linked Data

• dbSNP Id: rs747078135
• ExAC: 11:57379339 C / T
• gnomAD v2: 11-57379339-C-T
• gnomAD v4: 11-57611866-C-T
• MyVariant Identifiers: chr11:g.57379339C>T (hg19) ; chr11:g.57611866C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611866C>T , CM000673.2:g.57611866C>T	GRCh38
NC_000011.9:g.57379339C>T , CM000673.1:g.57379339C>T	GRCh37
NC_000011.8:g.57135915C>T	NCBI36
NG_009625.1:g.19313C>T , LRG_105:g.19313C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1179C>T MANE Select	ENSP00000278407.4:p.Pro393=
ENST00000528996.2:c.*76C>T	ENSP00000431226.2:n.*76C>T
ENST00000531605.2:c.*955C>T	ENSP00000503752.1:n.*955C>T
ENST00000619430.2:c.975C>T	ENSP00000478572.2:p.Pro325=
ENST00000676670.1:c.1179C>T	ENSP00000504807.1:p.Pro393=
ENST00000676741.1:n.2261C>T
ENST00000677624.1:c.*599C>T	ENSP00000503979.1:n.*599C>T
ENST00000677625.1:c.1125C>T	ENSP00000502857.1:p.Pro375=
ENST00000677856.1:n.1432C>T
ENST00000677915.1:c.*76C>T	ENSP00000503118.1:n.*76C>T
ENST00000678533.1:c.*733C>T	ENSP00000503873.1:n.*733C>T
ENST00000678592.1:c.*119C>T	ENSP00000504424.1:n.*119C>T
ENST00000278407.8:c.1179C>T	ENSP00000278407.4:p.Pro393=
ENST00000340687.10:c.1068C>T	ENSP00000341861.6:p.Pro356=
ENST00000378323.8:c.1194C>T	ENSP00000367574.4:p.Pro398=
ENST00000378324.6:c.1023C>T	ENSP00000367575.2:p.Pro341=
ENST00000403558.1:c.1308C>T	ENSP00000384420.1:p.Pro436=
ENST00000528996.1:c.380C>T	ENSP00000431226.1:n.380C>T
ENST00000530113.1:n.636C>T
ENST00000531133.5:c.680C>T	ENSP00000435431.1:n.680C>T
ENST00000531797.5:c.*204C>T	ENSP00000432554.1:n.*204C>T
ENST00000619430.1:c.349-39C>T	ENSP00000478572.1:n.349-39C>T
NM_000062.2:c.1179C>T , LRG_105t1:c.1179C>T	NP_000053.2:p.Pro393=
NM_001032295.1:c.1179C>T	NP_001027466.1:p.Pro393=
NM_000062.3:c.1179C>T MANE Select	NP_000053.2:p.Pro393=
NM_001032295.2:c.1179C>T	NP_001027466.1:p.Pro393=