Canonical Allele Identifier: CA474806891

Gene: SERPING1

Linked Data

• gnomAD v4: 11-57614485-G-C
• MyVariant Identifiers: chr11:g.57381958G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614485G>C , CM000673.2:g.57614485G>C	GRCh38
NC_000011.9:g.57381958G>C , CM000673.1:g.57381958G>C	GRCh37
NC_000011.8:g.57138534G>C	NCBI36
NG_009625.1:g.21932G>C , LRG_105:g.21932G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1407G>C MANE Select	ENSP00000278407.4:p.Leu469=
ENST00000528996.2:c.*304G>C	ENSP00000431226.2:n.*304G>C
ENST00000531605.2:c.*1183G>C	ENSP00000503752.1:n.*1183G>C
ENST00000619430.2:c.1203G>C	ENSP00000478572.2:p.Leu401=
ENST00000676670.1:c.1407G>C	ENSP00000504807.1:p.Leu469=
ENST00000676741.1:n.2489G>C
ENST00000677624.1:c.*827G>C	ENSP00000503979.1:n.*827G>C
ENST00000677625.1:c.1353G>C	ENSP00000502857.1:p.Leu451=
ENST00000677856.1:n.1660G>C
ENST00000677915.1:c.*304G>C	ENSP00000503118.1:n.*304G>C
ENST00000678533.1:c.*961G>C	ENSP00000503873.1:n.*961G>C
ENST00000678592.1:c.*347G>C	ENSP00000504424.1:n.*347G>C
ENST00000278407.8:c.1407G>C	ENSP00000278407.4:p.Leu469=
ENST00000340687.10:c.1296G>C	ENSP00000341861.6:p.Leu432=
ENST00000378323.8:c.1422G>C	ENSP00000367574.4:p.Leu474=
ENST00000378324.6:c.1251G>C	ENSP00000367575.2:p.Leu417=
ENST00000403558.1:c.1536G>C	ENSP00000384420.1:p.Leu512=
ENST00000528996.1:c.608G>C	ENSP00000431226.1:n.608G>C
ENST00000530113.1:n.864G>C
ENST00000531133.5:c.908G>C	ENSP00000435431.1:n.908G>C
ENST00000531797.5:c.*432G>C	ENSP00000432554.1:n.*432G>C
ENST00000619430.1:c.538G>C	ENSP00000478572.1:n.538G>C
NM_000062.2:c.1407G>C , LRG_105t1:c.1407G>C	NP_000053.2:p.Leu469=
NM_001032295.1:c.1407G>C	NP_001027466.1:p.Leu469=
NM_000062.3:c.1407G>C MANE Select	NP_000053.2:p.Leu469=
NM_001032295.2:c.1407G>C	NP_001027466.1:p.Leu469=