Canonical Allele Identifier: CA1975539465
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57614654T= , CM000673.2:g.57614654T= GRCh38
NC_000011.9:g.57382127T= , CM000673.1:g.57382127T= GRCh37
NC_000011.8:g.57138703T= NCBI36
NG_009625.1:g.22101T= , LRG_105:g.22101T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.*73T= MANE Select ENSP00000278407.4:n.*73T=
ENST00000528996.2:c.*473T= ENSP00000431226.2:n.*473T=
ENST00000531605.2:c.*1352T= ENSP00000503752.1:n.*1352T=
ENST00000619430.2:c.*73T= ENSP00000478572.2:n.*73T=
ENST00000676670.1:c.*15+58T= ENSP00000504807.1:n.*15+58T=
ENST00000676741.1:n.2658T=
ENST00000677624.1:c.*996T= ENSP00000503979.1:n.*996T=
ENST00000677625.1:c.*73T= ENSP00000502857.1:n.*73T=
ENST00000677856.1:n.1829T=
ENST00000677915.1:c.*473T= ENSP00000503118.1:n.*473T=
ENST00000678533.1:c.*1072+58T= ENSP00000503873.1:n.*1072+58T=
ENST00000678592.1:c.*516T= ENSP00000504424.1:n.*516T=
ENST00000278407.8:c.*73T= ENSP00000278407.4:n.*73T=
ENST00000340687.10:c.*73T= ENSP00000341861.6:n.*73T=
ENST00000378323.8:c.*73T= ENSP00000367574.4:n.*73T=
ENST00000378324.6:c.*73T= ENSP00000367575.2:n.*73T=
ENST00000403558.1:c.*73T= ENSP00000384420.1:n.*73T=
ENST00000528996.1:c.777T= ENSP00000431226.1:n.777T=
ENST00000531797.5:c.*601T= ENSP00000432554.1:n.*601T=
NM_000062.2:c.*73T= , LRG_105t1:c.*73T= NP_000053.2:n.*73T=
NM_001032295.1:c.*73T= NP_001027466.1:n.*73T=
NM_000062.3:c.*73T= MANE Select NP_000053.2:n.*73T=
NM_001032295.2:c.*73T= NP_001027466.1:n.*73T=