Canonical Allele Identifier: CA474567673

Gene: SERPING1

Linked Data

• gnomAD v4: 11-57611767-C-G
• MyVariant Identifiers: chr11:g.57379240C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611767C>G , CM000673.2:g.57611767C>G	GRCh38
NC_000011.9:g.57379240C>G , CM000673.1:g.57379240C>G	GRCh37
NC_000011.8:g.57135816C>G	NCBI36
NG_009625.1:g.19214C>G , LRG_105:g.19214C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1080C>G MANE Select	ENSP00000278407.4:p.Pro360=
ENST00000528996.2:c.100C>G	ENSP00000431226.2:p.Pro34Ala
ENST00000531605.2:c.*856C>G	ENSP00000503752.1:n.*856C>G
ENST00000619430.2:c.876C>G	ENSP00000478572.2:p.Pro292=
ENST00000676670.1:c.1080C>G	ENSP00000504807.1:p.Pro360=
ENST00000676741.1:n.2162C>G
ENST00000677624.1:c.*500C>G	ENSP00000503979.1:n.*500C>G
ENST00000677625.1:c.1030-4C>G	ENSP00000502857.1:n.1030-4C>G
ENST00000677856.1:n.1333C>G
ENST00000677915.1:c.736C>G	ENSP00000503118.1:p.Pro246Ala
ENST00000678533.1:c.*634C>G	ENSP00000503873.1:n.*634C>G
ENST00000678592.1:c.*20C>G	ENSP00000504424.1:n.*20C>G
ENST00000278407.8:c.1080C>G	ENSP00000278407.4:p.Pro360=
ENST00000340687.10:c.1030-61C>G	ENSP00000341861.6:n.1030-61C>G
ENST00000378323.8:c.1095C>G	ENSP00000367574.4:p.Pro365=
ENST00000378324.6:c.924C>G	ENSP00000367575.2:p.Pro308=
ENST00000403558.1:c.1209C>G	ENSP00000384420.1:p.Pro403=
ENST00000528996.1:c.281C>G	ENSP00000431226.1:n.281C>G
ENST00000530113.1:n.537C>G
ENST00000531133.5:c.581C>G	ENSP00000435431.1:n.581C>G
ENST00000531797.5:c.*105C>G	ENSP00000432554.1:n.*105C>G
ENST00000619430.1:c.349-138C>G	ENSP00000478572.1:n.349-138C>G
NM_000062.2:c.1080C>G , LRG_105t1:c.1080C>G	NP_000053.2:p.Pro360=
NM_001032295.1:c.1080C>G	NP_001027466.1:p.Pro360=
NM_000062.3:c.1080C>G MANE Select	NP_000053.2:p.Pro360=
NM_001032295.2:c.1080C>G	NP_001027466.1:p.Pro360=