Canonical Allele Identifier: CA380702537

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57379236T>C (hg19) ; chr11:g.57611763T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611763T>C , CM000673.2:g.57611763T>C	GRCh38
NC_000011.9:g.57379236T>C , CM000673.1:g.57379236T>C	GRCh37
NC_000011.8:g.57135812T>C	NCBI36
NG_009625.1:g.19210T>C , LRG_105:g.19210T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1076T>C MANE Select	ENSP00000278407.4:p.Val359Ala
ENST00000528996.2:c.96T>C	ENSP00000431226.2:p.Gly32=
ENST00000531605.2:c.*852T>C	ENSP00000503752.1:n.*852T>C
ENST00000619430.2:c.872T>C	ENSP00000478572.2:p.Val291Ala
ENST00000676670.1:c.1076T>C	ENSP00000504807.1:p.Val359Ala
ENST00000676741.1:n.2158T>C
ENST00000677624.1:c.*496T>C	ENSP00000503979.1:n.*496T>C
ENST00000677625.1:c.1030-8T>C	ENSP00000502857.1:n.1030-8T>C
ENST00000677856.1:n.1329T>C
ENST00000677915.1:c.732T>C	ENSP00000503118.1:p.Gly244=
ENST00000678533.1:c.*630T>C	ENSP00000503873.1:n.*630T>C
ENST00000678592.1:c.*16T>C	ENSP00000504424.1:n.*16T>C
ENST00000278407.8:c.1076T>C	ENSP00000278407.4:p.Val359Ala
ENST00000340687.10:c.1030-65T>C	ENSP00000341861.6:n.1030-65T>C
ENST00000378323.8:c.1091T>C	ENSP00000367574.4:p.Val364Ala
ENST00000378324.6:c.920T>C	ENSP00000367575.2:p.Val307Ala
ENST00000403558.1:c.1205T>C	ENSP00000384420.1:p.Val402Ala
ENST00000528996.1:c.277T>C	ENSP00000431226.1:n.277T>C
ENST00000530113.1:n.533T>C
ENST00000531133.5:c.577T>C	ENSP00000435431.1:n.577T>C
ENST00000531797.5:c.*101T>C	ENSP00000432554.1:n.*101T>C
ENST00000619430.1:c.349-142T>C	ENSP00000478572.1:n.349-142T>C
NM_000062.2:c.1076T>C , LRG_105t1:c.1076T>C	NP_000053.2:p.Val359Ala
NM_001032295.1:c.1076T>C	NP_001027466.1:p.Val359Ala
NM_000062.3:c.1076T>C MANE Select	NP_000053.2:p.Val359Ala
NM_001032295.2:c.1076T>C	NP_001027466.1:p.Val359Ala