Canonical Allele Identifier: CA2695214129

Gene: SERPING1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57606202_57606205del , CM000673.2:g.57606202_57606205del	GRCh38
NC_000011.9:g.57373675_57373678del , CM000673.1:g.57373675_57373678del	GRCh37
NC_000011.8:g.57130251_57130254del	NCBI36
NG_009625.1:g.13649_13652del , LRG_105:g.13649_13652del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.878_881del MANE Select	ENSP00000278407.4:p.Ile293ThrfsTer2
ENST00000528996.2:c.59-5524_59-5521del	ENSP00000431226.2:n.59-5524_59-5521del
ENST00000531605.2:c.*654_*657del	ENSP00000503752.1:n.*654_*657del
ENST00000619430.2:c.686-206_686-203del	ENSP00000478572.2:n.686-206_686-203del
ENST00000676670.1:c.878_881del	ENSP00000504807.1:p.Ile293ThrfsTer2
ENST00000676741.1:n.1960_1963del
ENST00000677624.1:c.*298_*301del	ENSP00000503979.1:n.*298_*301del
ENST00000677625.1:c.878_881del	ENSP00000502857.1:p.Ile293ThrfsTer2
ENST00000677856.1:n.937_940del
ENST00000677915.1:c.685+4033_685+4036del	ENSP00000503118.1:n.685+4033_685+4036del
ENST00000678533.1:c.*432_*435del	ENSP00000503873.1:n.*432_*435del
ENST00000678592.1:c.878_881del	ENSP00000504424.1:p.Ile293ThrfsTer2
ENST00000278407.8:c.878_881del	ENSP00000278407.4:p.Ile293ThrfsTer2
ENST00000340687.10:c.878_881del	ENSP00000341861.6:p.Ile293ThrfsTer2
ENST00000378323.8:c.893_896del	ENSP00000367574.4:p.Ile298ThrfsTer2
ENST00000378324.6:c.722_725del	ENSP00000367575.2:p.Ile241ThrfsTer2
ENST00000403558.1:c.980_983del	ENSP00000384420.1:p.Ile327ThrfsTer2
ENST00000531133.5:c.379_382del	ENSP00000435431.1:n.379_382del
ENST00000531797.5:c.*54+4033_*54+4036del	ENSP00000432554.1:n.*54+4033_*54+4036del
ENST00000619430.1:c.349-5703_349-5700del	ENSP00000478572.1:n.349-5703_349-5700del
NM_000062.2:c.878_881del , LRG_105t1:c.878_881del	NP_000053.2:p.Ile293ThrfsTer2
NM_001032295.1:c.878_881del	NP_001027466.1:p.Ile293ThrfsTer2
NM_000062.3:c.878_881del MANE Select	NP_000053.2:p.Ile293ThrfsTer2
NM_001032295.2:c.878_881del	NP_001027466.1:p.Ile293ThrfsTer2