Canonical Allele Identifier: CA1975537123
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57611851G= , CM000673.2:g.57611851G= GRCh38
NC_000011.9:g.57379324G= , CM000673.1:g.57379324G= GRCh37
NC_000011.8:g.57135900G= NCBI36
NG_009625.1:g.19298G= , LRG_105:g.19298G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.1164G= MANE Select ENSP00000278407.4:p.Met388=
ENST00000528996.2:c.*61G= ENSP00000431226.2:n.*61G=
ENST00000531605.2:c.*940G= ENSP00000503752.1:n.*940G=
ENST00000619430.2:c.960G= ENSP00000478572.2:p.Met320=
ENST00000676670.1:c.1164G= ENSP00000504807.1:p.Met388=
ENST00000676741.1:n.2246G=
ENST00000677624.1:c.*584G= ENSP00000503979.1:n.*584G=
ENST00000677625.1:c.1110G= ENSP00000502857.1:p.Met370=
ENST00000677856.1:n.1417G=
ENST00000677915.1:c.*61G= ENSP00000503118.1:n.*61G=
ENST00000678533.1:c.*718G= ENSP00000503873.1:n.*718G=
ENST00000678592.1:c.*104G= ENSP00000504424.1:n.*104G=
ENST00000278407.8:c.1164G= ENSP00000278407.4:p.Met388=
ENST00000340687.10:c.1053G= ENSP00000341861.6:p.Met351=
ENST00000378323.8:c.1179G= ENSP00000367574.4:p.Met393=
ENST00000378324.6:c.1008G= ENSP00000367575.2:p.Met336=
ENST00000403558.1:c.1293G= ENSP00000384420.1:p.Met431=
ENST00000528996.1:c.365G= ENSP00000431226.1:n.365G=
ENST00000530113.1:n.621G=
ENST00000531133.5:c.665G= ENSP00000435431.1:n.665G=
ENST00000531797.5:c.*189G= ENSP00000432554.1:n.*189G=
ENST00000619430.1:c.349-54G= ENSP00000478572.1:n.349-54G=
NM_000062.2:c.1164G= , LRG_105t1:c.1164G= NP_000053.2:p.Met388=
NM_001032295.1:c.1164G= NP_001027466.1:p.Met388=
NM_000062.3:c.1164G= MANE Select NP_000053.2:p.Met388=
NM_001032295.2:c.1164G= NP_001027466.1:p.Met388=