Canonical Allele Identifier: CA1975537125
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57611851_57611858delinsGTCCAAGT , CM000673.2:g.57611851_57611858delinsGTCCAAGT GRCh38
NC_000011.9:g.57379324_57379331delinsGTCCAAGT , CM000673.1:g.57379324_57379331delinsGTCCAAGT GRCh37
NC_000011.8:g.57135900_57135907delinsGTCCAAGT NCBI36
NG_009625.1:g.19298_19305delinsGTCCAAGT , LRG_105:g.19298_19305delinsGTCCAAGT

Transcript Alleles

HGVS Amino-acid change
ENST00000278407.9:c.1164_1171delinsGTCCAAGT MANE Select ENSP00000278407.4:p.Met388=
ENST00000528996.2:c.*61_*68delinsGTCCAAGT ENSP00000431226.2:n.*61_*68delinsGTCCAAGT
ENST00000531605.2:c.*940_*947delinsGTCCAAGT ENSP00000503752.1:n.*940_*947delinsGTCCAAGT
ENST00000619430.2:c.960_967delinsGTCCAAGT ENSP00000478572.2:p.Met320=
ENST00000676670.1:c.1164_1171delinsGTCCAAGT ENSP00000504807.1:p.Met388=
ENST00000676741.1:n.2246_2253delinsGTCCAAGT
ENST00000677624.1:c.*584_*591delinsGTCCAAGT ENSP00000503979.1:n.*584_*591delinsGTCCAAGT
ENST00000677625.1:c.1110_1117delinsGTCCAAGT ENSP00000502857.1:p.Met370=
ENST00000677856.1:n.1417_1424delinsGTCCAAGT
ENST00000677915.1:c.*61_*68delinsGTCCAAGT ENSP00000503118.1:n.*61_*68delinsGTCCAAGT
ENST00000678533.1:c.*718_*725delinsGTCCAAGT ENSP00000503873.1:n.*718_*725delinsGTCCAAGT
ENST00000678592.1:c.*104_*111delinsGTCCAAGT ENSP00000504424.1:n.*104_*111delinsGTCCAAGT
ENST00000278407.8:c.1164_1171delinsGTCCAAGT ENSP00000278407.4:p.Met388=
ENST00000340687.10:c.1053_1060delinsGTCCAAGT ENSP00000341861.6:p.Met351=
ENST00000378323.8:c.1179_1186delinsGTCCAAGT ENSP00000367574.4:p.Met393=
ENST00000378324.6:c.1008_1015delinsGTCCAAGT ENSP00000367575.2:p.Met336=
ENST00000403558.1:c.1293_1300delinsGTCCAAGT ENSP00000384420.1:p.Met431=
ENST00000528996.1:c.365_372delinsGTCCAAGT ENSP00000431226.1:n.365_372delinsGTCCAAGT
ENST00000530113.1:n.621_628delinsGTCCAAGT
ENST00000531133.5:c.665_672delinsGTCCAAGT ENSP00000435431.1:n.665_672delinsGTCCAAGT
ENST00000531797.5:c.*189_*196delinsGTCCAAGT ENSP00000432554.1:n.*189_*196delinsGTCCAAGT
ENST00000619430.1:c.349-54_349-47delinsGTCCAAGT ENSP00000478572.1:n.349-54_349-47delinsGTCCAAGT
NM_000062.2:c.1164_1171delinsGTCCAAGT , LRG_105t1:c.1164_1171delinsGTCCAAGT NP_000053.2:p.Met388=
NM_001032295.1:c.1164_1171delinsGTCCAAGT NP_001027466.1:p.Met388=
NM_000062.3:c.1164_1171delinsGTCCAAGT MANE Select NP_000053.2:p.Met388=
NM_001032295.2:c.1164_1171delinsGTCCAAGT NP_001027466.1:p.Met388=