Canonical Allele Identifier: CA599805397

Gene: SERPING1

Linked Data

• dbSNP Id: rs1432652840
• gnomAD v2: 11-57373700-T-C
• gnomAD v3: 11-57606227-T-C
• gnomAD v4: 11-57606227-T-C
• MyVariant Identifiers: chr11:g.57373700T>C (hg19) ; chr11:g.57606227T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57606227T>C , CM000673.2:g.57606227T>C	GRCh38
NC_000011.9:g.57373700T>C , CM000673.1:g.57373700T>C	GRCh37
NC_000011.8:g.57130276T>C	NCBI36
NG_009625.1:g.13674T>C , LRG_105:g.13674T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.889+14T>C MANE Select	ENSP00000278407.4:n.889+14T>C
ENST00000528996.2:c.59-5499T>C	ENSP00000431226.2:n.59-5499T>C
ENST00000531605.2:c.*665+14T>C	ENSP00000503752.1:n.*665+14T>C
ENST00000619430.2:c.686-181T>C	ENSP00000478572.2:n.686-181T>C
ENST00000676670.1:c.889+14T>C	ENSP00000504807.1:n.889+14T>C
ENST00000676741.1:n.1971+14T>C
ENST00000677624.1:c.*309+14T>C	ENSP00000503979.1:n.*309+14T>C
ENST00000677625.1:c.889+14T>C	ENSP00000502857.1:n.889+14T>C
ENST00000677856.1:n.962T>C
ENST00000677915.1:c.685+4058T>C	ENSP00000503118.1:n.685+4058T>C
ENST00000678533.1:c.*443+14T>C	ENSP00000503873.1:n.*443+14T>C
ENST00000678592.1:c.889+14T>C	ENSP00000504424.1:n.889+14T>C
ENST00000278407.8:c.889+14T>C	ENSP00000278407.4:n.889+14T>C
ENST00000340687.10:c.889+14T>C	ENSP00000341861.6:n.889+14T>C
ENST00000378323.8:c.904+14T>C	ENSP00000367574.4:n.904+14T>C
ENST00000378324.6:c.733+14T>C	ENSP00000367575.2:n.733+14T>C
ENST00000403558.1:c.991+14T>C	ENSP00000384420.1:n.991+14T>C
ENST00000531133.5:c.390+14T>C	ENSP00000435431.1:n.390+14T>C
ENST00000531797.5:c.*54+4058T>C	ENSP00000432554.1:n.*54+4058T>C
ENST00000619430.1:c.349-5678T>C	ENSP00000478572.1:n.349-5678T>C
NM_000062.2:c.889+14T>C , LRG_105t1:c.889+14T>C	NP_000053.2:n.889+14T>C
NM_001032295.1:c.889+14T>C	NP_001027466.1:n.889+14T>C
NM_000062.3:c.889+14T>C MANE Select	NP_000053.2:n.889+14T>C
NM_001032295.2:c.889+14T>C	NP_001027466.1:n.889+14T>C