Canonical Allele Identifier: CA380699059

Gene: SERPING1

Linked Data

• gnomAD v4: 11-57606091-A-C
• MyVariant Identifiers: chr11:g.57373564A>C (hg19) ; chr11:g.57606091A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57606091A>C , CM000673.2:g.57606091A>C	GRCh38
NC_000011.9:g.57373564A>C , CM000673.1:g.57373564A>C	GRCh37
NC_000011.8:g.57130140A>C	NCBI36
NG_009625.1:g.13538A>C , LRG_105:g.13538A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.767A>C MANE Select	ENSP00000278407.4:p.Asp256Ala
ENST00000528996.2:c.59-5635A>C	ENSP00000431226.2:n.59-5635A>C
ENST00000531605.2:c.*543A>C	ENSP00000503752.1:n.*543A>C
ENST00000619430.2:c.686-317A>C	ENSP00000478572.2:n.686-317A>C
ENST00000676670.1:c.767A>C	ENSP00000504807.1:p.Asp256Ala
ENST00000676741.1:n.1849A>C
ENST00000677624.1:c.*187A>C	ENSP00000503979.1:n.*187A>C
ENST00000677625.1:c.767A>C	ENSP00000502857.1:p.Asp256Ala
ENST00000677856.1:n.826A>C
ENST00000677915.1:c.685+3922A>C	ENSP00000503118.1:n.685+3922A>C
ENST00000678533.1:c.*321A>C	ENSP00000503873.1:n.*321A>C
ENST00000678592.1:c.767A>C	ENSP00000504424.1:p.Asp256Ala
ENST00000278407.8:c.767A>C	ENSP00000278407.4:p.Asp256Ala
ENST00000340687.10:c.767A>C	ENSP00000341861.6:p.Asp256Ala
ENST00000378323.8:c.782A>C	ENSP00000367574.4:p.Asp261Ala
ENST00000378324.6:c.611A>C	ENSP00000367575.2:p.Asp204Ala
ENST00000403558.1:c.869A>C	ENSP00000384420.1:p.Asp290Ala
ENST00000531133.5:c.268A>C	ENSP00000435431.1:n.268A>C
ENST00000531797.5:c.*54+3922A>C	ENSP00000432554.1:n.*54+3922A>C
ENST00000619430.1:c.349-5814A>C	ENSP00000478572.1:n.349-5814A>C
NM_000062.2:c.767A>C , LRG_105t1:c.767A>C	NP_000053.2:p.Asp256Ala
NM_001032295.1:c.767A>C	NP_001027466.1:p.Asp256Ala
NM_000062.3:c.767A>C MANE Select	NP_000053.2:p.Asp256Ala
NM_001032295.2:c.767A>C	NP_001027466.1:p.Asp256Ala