Canonical Allele Identifier: CA380703111

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57379325T>G (hg19) ; chr11:g.57611852T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611852T>G , CM000673.2:g.57611852T>G	GRCh38
NC_000011.9:g.57379325T>G , CM000673.1:g.57379325T>G	GRCh37
NC_000011.8:g.57135901T>G	NCBI36
NG_009625.1:g.19299T>G , LRG_105:g.19299T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1165T>G MANE Select	ENSP00000278407.4:p.Ser389Ala
ENST00000528996.2:c.*62T>G	ENSP00000431226.2:n.*62T>G
ENST00000531605.2:c.*941T>G	ENSP00000503752.1:n.*941T>G
ENST00000619430.2:c.961T>G	ENSP00000478572.2:p.Ser321Ala
ENST00000676670.1:c.1165T>G	ENSP00000504807.1:p.Ser389Ala
ENST00000676741.1:n.2247T>G
ENST00000677624.1:c.*585T>G	ENSP00000503979.1:n.*585T>G
ENST00000677625.1:c.1111T>G	ENSP00000502857.1:p.Ser371Ala
ENST00000677856.1:n.1418T>G
ENST00000677915.1:c.*62T>G	ENSP00000503118.1:n.*62T>G
ENST00000678533.1:c.*719T>G	ENSP00000503873.1:n.*719T>G
ENST00000678592.1:c.*105T>G	ENSP00000504424.1:n.*105T>G
ENST00000278407.8:c.1165T>G	ENSP00000278407.4:p.Ser389Ala
ENST00000340687.10:c.1054T>G	ENSP00000341861.6:p.Ser352Ala
ENST00000378323.8:c.1180T>G	ENSP00000367574.4:p.Ser394Ala
ENST00000378324.6:c.1009T>G	ENSP00000367575.2:p.Ser337Ala
ENST00000403558.1:c.1294T>G	ENSP00000384420.1:p.Ser432Ala
ENST00000528996.1:c.366T>G	ENSP00000431226.1:n.366T>G
ENST00000530113.1:n.622T>G
ENST00000531133.5:c.666T>G	ENSP00000435431.1:n.666T>G
ENST00000531797.5:c.*190T>G	ENSP00000432554.1:n.*190T>G
ENST00000619430.1:c.349-53T>G	ENSP00000478572.1:n.349-53T>G
NM_000062.2:c.1165T>G , LRG_105t1:c.1165T>G	NP_000053.2:p.Ser389Ala
NM_001032295.1:c.1165T>G	NP_001027466.1:p.Ser389Ala
NM_000062.3:c.1165T>G MANE Select	NP_000053.2:p.Ser389Ala
NM_001032295.2:c.1165T>G	NP_001027466.1:p.Ser389Ala