Canonical Allele Identifier: CA474566629

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57373673T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57606200T>C , CM000673.2:g.57606200T>C	GRCh38
NC_000011.9:g.57373673T>C , CM000673.1:g.57373673T>C	GRCh37
NC_000011.8:g.57130249T>C	NCBI36
NG_009625.1:g.13647T>C , LRG_105:g.13647T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.876T>C MANE Select	ENSP00000278407.4:p.Ala292=
ENST00000528996.2:c.59-5526T>C	ENSP00000431226.2:n.59-5526T>C
ENST00000531605.2:c.*652T>C	ENSP00000503752.1:n.*652T>C
ENST00000619430.2:c.686-208T>C	ENSP00000478572.2:n.686-208T>C
ENST00000676670.1:c.876T>C	ENSP00000504807.1:p.Ala292=
ENST00000676741.1:n.1958T>C
ENST00000677624.1:c.*296T>C	ENSP00000503979.1:n.*296T>C
ENST00000677625.1:c.876T>C	ENSP00000502857.1:p.Ala292=
ENST00000677856.1:n.935T>C
ENST00000677915.1:c.685+4031T>C	ENSP00000503118.1:n.685+4031T>C
ENST00000678533.1:c.*430T>C	ENSP00000503873.1:n.*430T>C
ENST00000678592.1:c.876T>C	ENSP00000504424.1:p.Ala292=
ENST00000278407.8:c.876T>C	ENSP00000278407.4:p.Ala292=
ENST00000340687.10:c.876T>C	ENSP00000341861.6:p.Ala292=
ENST00000378323.8:c.891T>C	ENSP00000367574.4:p.Ala297=
ENST00000378324.6:c.720T>C	ENSP00000367575.2:p.Ala240=
ENST00000403558.1:c.978T>C	ENSP00000384420.1:p.Ala326=
ENST00000531133.5:c.377T>C	ENSP00000435431.1:n.377T>C
ENST00000531797.5:c.*54+4031T>C	ENSP00000432554.1:n.*54+4031T>C
ENST00000619430.1:c.349-5705T>C	ENSP00000478572.1:n.349-5705T>C
NM_000062.2:c.876T>C , LRG_105t1:c.876T>C	NP_000053.2:p.Ala292=
NM_001032295.1:c.876T>C	NP_001027466.1:p.Ala292=
NM_000062.3:c.876T>C MANE Select	NP_000053.2:p.Ala292=
NM_001032295.2:c.876T>C	NP_001027466.1:p.Ala292=