Canonical Allele Identifier: CA1975537148

Gene: SERPING1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611866_57611867delinsCA , CM000673.2:g.57611866_57611867delinsCA	GRCh38
NC_000011.9:g.57379339_57379340delinsCA , CM000673.1:g.57379339_57379340delinsCA	GRCh37
NC_000011.8:g.57135915_57135916delinsCA	NCBI36
NG_009625.1:g.19313_19314delinsCA , LRG_105:g.19313_19314delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1179_1180delinsCA MANE Select	ENSP00000278407.4:p.Pro393=
ENST00000528996.2:c.*76_*77delinsCA	ENSP00000431226.2:n.*76_*77delinsCA
ENST00000531605.2:c.*955_*956delinsCA	ENSP00000503752.1:n.*955_*956delinsCA
ENST00000619430.2:c.975_976delinsCA	ENSP00000478572.2:p.Pro325=
ENST00000676670.1:c.1179_1180delinsCA	ENSP00000504807.1:p.Pro393=
ENST00000676741.1:n.2261_2262delinsCA
ENST00000677624.1:c.*599_*600delinsCA	ENSP00000503979.1:n.*599_*600delinsCA
ENST00000677625.1:c.1125_1126delinsCA	ENSP00000502857.1:p.Pro375=
ENST00000677856.1:n.1432_1433delinsCA
ENST00000677915.1:c.*76_*77delinsCA	ENSP00000503118.1:n.*76_*77delinsCA
ENST00000678533.1:c.*733_*734delinsCA	ENSP00000503873.1:n.*733_*734delinsCA
ENST00000678592.1:c.*119_*120delinsCA	ENSP00000504424.1:n.*119_*120delinsCA
ENST00000278407.8:c.1179_1180delinsCA	ENSP00000278407.4:p.Pro393=
ENST00000340687.10:c.1068_1069delinsCA	ENSP00000341861.6:p.Pro356=
ENST00000378323.8:c.1194_1195delinsCA	ENSP00000367574.4:p.Pro398=
ENST00000378324.6:c.1023_1024delinsCA	ENSP00000367575.2:p.Pro341=
ENST00000403558.1:c.1308_1309delinsCA	ENSP00000384420.1:p.Pro436=
ENST00000528996.1:c.380_381delinsCA	ENSP00000431226.1:n.380_381delinsCA
ENST00000530113.1:n.636_637delinsCA
ENST00000531133.5:c.680_681delinsCA	ENSP00000435431.1:n.680_681delinsCA
ENST00000531797.5:c.*204_*205delinsCA	ENSP00000432554.1:n.*204_*205delinsCA
ENST00000619430.1:c.349-39_349-38delinsCA	ENSP00000478572.1:n.349-39_349-38delinsCA
NM_000062.2:c.1179_1180delinsCA , LRG_105t1:c.1179_1180delinsCA	NP_000053.2:p.Pro393=
NM_001032295.1:c.1179_1180delinsCA	NP_001027466.1:p.Pro393=
NM_000062.3:c.1179_1180delinsCA MANE Select	NP_000053.2:p.Pro393=
NM_001032295.2:c.1179_1180delinsCA	NP_001027466.1:p.Pro393=