Canonical Allele Identifier: CA1975531526

Gene: SERPING1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57606177_57606178delinsAC , CM000673.2:g.57606177_57606178delinsAC	GRCh38
NC_000011.9:g.57373650_57373651delinsAC , CM000673.1:g.57373650_57373651delinsAC	GRCh37
NC_000011.8:g.57130226_57130227delinsAC	NCBI36
NG_009625.1:g.13624_13625delinsAC , LRG_105:g.13624_13625delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.853_854delinsAC MANE Select	ENSP00000278407.4:p.Thr285=
ENST00000528996.2:c.59-5549_59-5548delinsAC	ENSP00000431226.2:n.59-5549_59-5548delinsAC
ENST00000531605.2:c.*629_*630delinsAC	ENSP00000503752.1:n.*629_*630delinsAC
ENST00000619430.2:c.686-231_686-230delinsAC	ENSP00000478572.2:n.686-231_686-230delinsAC
ENST00000676670.1:c.853_854delinsAC	ENSP00000504807.1:p.Thr285=
ENST00000676741.1:n.1935_1936delinsAC
ENST00000677624.1:c.*273_*274delinsAC	ENSP00000503979.1:n.*273_*274delinsAC
ENST00000677625.1:c.853_854delinsAC	ENSP00000502857.1:p.Thr285=
ENST00000677856.1:n.912_913delinsAC
ENST00000677915.1:c.685+4008_685+4009delinsAC	ENSP00000503118.1:n.685+4008_685+4009delinsAC
ENST00000678533.1:c.*407_*408delinsAC	ENSP00000503873.1:n.*407_*408delinsAC
ENST00000678592.1:c.853_854delinsAC	ENSP00000504424.1:p.Thr285=
ENST00000278407.8:c.853_854delinsAC	ENSP00000278407.4:p.Thr285=
ENST00000340687.10:c.853_854delinsAC	ENSP00000341861.6:p.Thr285=
ENST00000378323.8:c.868_869delinsAC	ENSP00000367574.4:p.Thr290=
ENST00000378324.6:c.697_698delinsAC	ENSP00000367575.2:p.Thr233=
ENST00000403558.1:c.955_956delinsAC	ENSP00000384420.1:p.Thr319=
ENST00000531133.5:c.354_355delinsAC	ENSP00000435431.1:n.354_355delinsAC
ENST00000531797.5:c.*54+4008_*54+4009delinsAC	ENSP00000432554.1:n.*54+4008_*54+4009delinsAC
ENST00000619430.1:c.349-5728_349-5727delinsAC	ENSP00000478572.1:n.349-5728_349-5727delinsAC
NM_000062.2:c.853_854delinsAC , LRG_105t1:c.853_854delinsAC	NP_000053.2:p.Thr285=
NM_001032295.1:c.853_854delinsAC	NP_001027466.1:p.Thr285=
NM_000062.3:c.853_854delinsAC MANE Select	NP_000053.2:p.Thr285=
NM_001032295.2:c.853_854delinsAC	NP_001027466.1:p.Thr285=