Canonical Allele Identifier: CA2695214093

Gene: SERPING1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57606104_57606128del , CM000673.2:g.57606104_57606128del	GRCh38
NC_000011.9:g.57373577_57373601del , CM000673.1:g.57373577_57373601del	GRCh37
NC_000011.8:g.57130153_57130177del	NCBI36
NG_009625.1:g.13551_13575del , LRG_105:g.13551_13575del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.780_804del MANE Select	ENSP00000278407.4:p.Leu261ThrfsTer10
ENST00000528996.2:c.59-5622_59-5598del	ENSP00000431226.2:n.59-5622_59-5598del
ENST00000531605.2:c.*556_*580del	ENSP00000503752.1:n.*556_*580del
ENST00000619430.2:c.686-304_686-280del	ENSP00000478572.2:n.686-304_686-280del
ENST00000676670.1:c.780_804del	ENSP00000504807.1:p.Leu261ThrfsTer10
ENST00000676741.1:n.1862_1886del
ENST00000677624.1:c.*200_*224del	ENSP00000503979.1:n.*200_*224del
ENST00000677625.1:c.780_804del	ENSP00000502857.1:p.Leu261ThrfsTer10
ENST00000677856.1:n.839_863del
ENST00000677915.1:c.685+3935_685+3959del	ENSP00000503118.1:n.685+3935_685+3959del
ENST00000678533.1:c.*334_*358del	ENSP00000503873.1:n.*334_*358del
ENST00000678592.1:c.780_804del	ENSP00000504424.1:p.Leu261ThrfsTer10
ENST00000278407.8:c.780_804del	ENSP00000278407.4:p.Leu261ThrfsTer10
ENST00000340687.10:c.780_804del	ENSP00000341861.6:p.Leu261ThrfsTer10
ENST00000378323.8:c.795_819del	ENSP00000367574.4:p.Leu266ThrfsTer10
ENST00000378324.6:c.624_648del	ENSP00000367575.2:p.Leu209ThrfsTer10
ENST00000403558.1:c.882_906del	ENSP00000384420.1:p.Leu295ThrfsTer10
ENST00000531133.5:c.281_305del	ENSP00000435431.1:n.281_305del
ENST00000531797.5:c.*54+3935_*54+3959del	ENSP00000432554.1:n.*54+3935_*54+3959del
ENST00000619430.1:c.349-5801_349-5777del	ENSP00000478572.1:n.349-5801_349-5777del
NM_000062.2:c.780_804del , LRG_105t1:c.780_804del	NP_000053.2:p.Leu261ThrfsTer10
NM_001032295.1:c.780_804del	NP_001027466.1:p.Leu261ThrfsTer10
NM_000062.3:c.780_804del MANE Select	NP_000053.2:p.Leu261ThrfsTer10
NM_001032295.2:c.780_804del	NP_001027466.1:p.Leu261ThrfsTer10