Canonical Allele Identifier: CA380699132

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57373573T>A (hg19) ; chr11:g.57606100T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57606100T>A , CM000673.2:g.57606100T>A	GRCh38
NC_000011.9:g.57373573T>A , CM000673.1:g.57373573T>A	GRCh37
NC_000011.8:g.57130149T>A	NCBI36
NG_009625.1:g.13547T>A , LRG_105:g.13547T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.776T>A MANE Select	ENSP00000278407.4:p.Leu259Ter
ENST00000528996.2:c.59-5626T>A	ENSP00000431226.2:n.59-5626T>A
ENST00000531605.2:c.*552T>A	ENSP00000503752.1:n.*552T>A
ENST00000619430.2:c.686-308T>A	ENSP00000478572.2:n.686-308T>A
ENST00000676670.1:c.776T>A	ENSP00000504807.1:p.Leu259Ter
ENST00000676741.1:n.1858T>A
ENST00000677624.1:c.*196T>A	ENSP00000503979.1:n.*196T>A
ENST00000677625.1:c.776T>A	ENSP00000502857.1:p.Leu259Ter
ENST00000677856.1:n.835T>A
ENST00000677915.1:c.685+3931T>A	ENSP00000503118.1:n.685+3931T>A
ENST00000678533.1:c.*330T>A	ENSP00000503873.1:n.*330T>A
ENST00000678592.1:c.776T>A	ENSP00000504424.1:p.Leu259Ter
ENST00000278407.8:c.776T>A	ENSP00000278407.4:p.Leu259Ter
ENST00000340687.10:c.776T>A	ENSP00000341861.6:p.Leu259Ter
ENST00000378323.8:c.791T>A	ENSP00000367574.4:p.Leu264Ter
ENST00000378324.6:c.620T>A	ENSP00000367575.2:p.Leu207Ter
ENST00000403558.1:c.878T>A	ENSP00000384420.1:p.Leu293Ter
ENST00000531133.5:c.277T>A	ENSP00000435431.1:n.277T>A
ENST00000531797.5:c.*54+3931T>A	ENSP00000432554.1:n.*54+3931T>A
ENST00000619430.1:c.349-5805T>A	ENSP00000478572.1:n.349-5805T>A
NM_000062.2:c.776T>A , LRG_105t1:c.776T>A	NP_000053.2:p.Leu259Ter
NM_001032295.1:c.776T>A	NP_001027466.1:p.Leu259Ter
NM_000062.3:c.776T>A MANE Select	NP_000053.2:p.Leu259Ter
NM_001032295.2:c.776T>A	NP_001027466.1:p.Leu259Ter