Canonical Allele Identifier: CA474565473

Gene: SERPING1

Linked Data

• gnomAD v4: 11-57600235-T-C
• MyVariant Identifiers: chr11:g.57367708T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57600235T>C , CM000673.2:g.57600235T>C	GRCh38
NC_000011.9:g.57367708T>C , CM000673.1:g.57367708T>C	GRCh37
NC_000011.8:g.57124284T>C	NCBI36
NG_009625.1:g.7682T>C , LRG_105:g.7682T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.408T>C MANE Select	ENSP00000278407.4:p.His136=
ENST00000528996.2:c.58+1907T>C	ENSP00000431226.2:n.58+1907T>C
ENST00000531605.2:c.52-1800T>C	ENSP00000503752.1:n.52-1800T>C
ENST00000619430.2:c.408T>C	ENSP00000478572.2:p.His136=
ENST00000676670.1:c.408T>C	ENSP00000504807.1:p.His136=
ENST00000676741.1:n.1490T>C
ENST00000677275.1:n.395T>C
ENST00000677624.1:c.408T>C	ENSP00000503979.1:p.His136=
ENST00000677625.1:c.408T>C	ENSP00000502857.1:p.His136=
ENST00000677856.1:n.467T>C
ENST00000677915.1:c.408T>C	ENSP00000503118.1:p.His136=
ENST00000678533.1:c.52-1800T>C	ENSP00000503873.1:n.52-1800T>C
ENST00000678592.1:c.408T>C	ENSP00000504424.1:p.His136=
ENST00000278407.8:c.408T>C	ENSP00000278407.4:p.His136=
ENST00000340687.10:c.408T>C	ENSP00000341861.6:p.His136=
ENST00000378323.8:c.423T>C	ENSP00000367574.4:p.His141=
ENST00000378324.6:c.252T>C	ENSP00000367575.2:p.His84=
ENST00000403558.1:c.510T>C	ENSP00000384420.1:p.His170=
ENST00000405496.5:c.408T>C	ENSP00000384561.1:p.His136=
ENST00000531133.5:c.52-1800T>C	ENSP00000435431.1:n.52-1800T>C
ENST00000531797.5:c.52-1800T>C	ENSP00000432554.1:n.52-1800T>C
ENST00000619430.1:c.348+60T>C	ENSP00000478572.1:n.348+60T>C
NM_000062.2:c.408T>C , LRG_105t1:c.408T>C	NP_000053.2:p.His136=
NM_001032295.1:c.408T>C	NP_001027466.1:p.His136=
NM_000062.3:c.408T>C MANE Select	NP_000053.2:p.His136=
NM_001032295.2:c.408T>C	NP_001027466.1:p.His136=