Canonical Allele Identifier: CA599805396

Gene: SERPING1

Linked Data

• dbSNP Id: rs1426218981
• gnomAD v2: 11-57373693-G-T
• gnomAD v4: 11-57606220-G-T
• MyVariant Identifiers: chr11:g.57373693G>T (hg19) ; chr11:g.57606220G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57606220G>T , CM000673.2:g.57606220G>T	GRCh38
NC_000011.9:g.57373693G>T , CM000673.1:g.57373693G>T	GRCh37
NC_000011.8:g.57130269G>T	NCBI36
NG_009625.1:g.13667G>T , LRG_105:g.13667G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.889+7G>T MANE Select	ENSP00000278407.4:n.889+7G>T
ENST00000528996.2:c.59-5506G>T	ENSP00000431226.2:n.59-5506G>T
ENST00000531605.2:c.*665+7G>T	ENSP00000503752.1:n.*665+7G>T
ENST00000619430.2:c.686-188G>T	ENSP00000478572.2:n.686-188G>T
ENST00000676670.1:c.889+7G>T	ENSP00000504807.1:n.889+7G>T
ENST00000676741.1:n.1971+7G>T
ENST00000677624.1:c.*309+7G>T	ENSP00000503979.1:n.*309+7G>T
ENST00000677625.1:c.889+7G>T	ENSP00000502857.1:n.889+7G>T
ENST00000677856.1:n.955G>T
ENST00000677915.1:c.685+4051G>T	ENSP00000503118.1:n.685+4051G>T
ENST00000678533.1:c.*443+7G>T	ENSP00000503873.1:n.*443+7G>T
ENST00000678592.1:c.889+7G>T	ENSP00000504424.1:n.889+7G>T
ENST00000278407.8:c.889+7G>T	ENSP00000278407.4:n.889+7G>T
ENST00000340687.10:c.889+7G>T	ENSP00000341861.6:n.889+7G>T
ENST00000378323.8:c.904+7G>T	ENSP00000367574.4:n.904+7G>T
ENST00000378324.6:c.733+7G>T	ENSP00000367575.2:n.733+7G>T
ENST00000403558.1:c.991+7G>T	ENSP00000384420.1:n.991+7G>T
ENST00000531133.5:c.390+7G>T	ENSP00000435431.1:n.390+7G>T
ENST00000531797.5:c.*54+4051G>T	ENSP00000432554.1:n.*54+4051G>T
ENST00000619430.1:c.349-5685G>T	ENSP00000478572.1:n.349-5685G>T
NM_000062.2:c.889+7G>T , LRG_105t1:c.889+7G>T	NP_000053.2:n.889+7G>T
NM_001032295.1:c.889+7G>T	NP_001027466.1:n.889+7G>T
NM_000062.3:c.889+7G>T MANE Select	NP_000053.2:n.889+7G>T
NM_001032295.2:c.889+7G>T	NP_001027466.1:n.889+7G>T