Canonical Allele Identifier: CA2695237342
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154966446_154966455delinsCT , CM000685.2:g.154966446_154966455delinsCT GRCh38
NC_000023.10:g.154194721_154194730delinsCT , CM000685.1:g.154194721_154194730delinsCT GRCh37
NC_000023.9:g.153847915_153847924delinsCT NCBI36
NG_011403.1:g.61269_61278delinsAG
NG_011403.2:g.61269_61278delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.1242_1251delinsAG MANE Select ENSP00000353393.4:p.Tyr414Ter
ENST00000647125.1:c.*1118_*1127delinsAG ENSP00000496062.1:n.*1118_*1127delinsAG
ENST00000360256.8:c.1242_1251delinsAG ENSP00000353393.4:p.Tyr414Ter
ENST00000483822.2:n.62_71delinsAG
NM_000132.3:c.1242_1251delinsAG NP_000123.1:p.Tyr414Ter
XM_011531126.1:c.1137_1146delinsAG XP_011529428.1:p.Tyr379Ter
NM_000132.4:c.1242_1251delinsAG MANE Select NP_000123.1:p.Tyr414Ter
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