Canonical Allele Identifier: CA2466828438
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904890_154904891delinsCA , CM000685.2:g.154904890_154904891delinsCA GRCh38
NC_000023.10:g.154133165_154133166delinsCA , CM000685.1:g.154133165_154133166delinsCA GRCh37
NC_000023.9:g.153786359_153786360delinsCA NCBI36
NG_011403.1:g.122833_122834delinsTG
NG_011403.2:g.122833_122834delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5506_5507delinsTG MANE Select ENSP00000353393.4:p.Trp1836=
ENST00000360256.8:c.5506_5507delinsTG ENSP00000353393.4:p.Trp1836=
NM_000132.3:c.5506_5507delinsTG NP_000123.1:p.Trp1836=
XM_011531126.1:c.5401_5402delinsTG XP_011529428.1:p.Trp1801=
NM_000132.4:c.5506_5507delinsTG MANE Select NP_000123.1:p.Trp1836=
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