Canonical Allele Identifier: CA2466849042
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154969490_154969491delinsCA , CM000685.2:g.154969490_154969491delinsCA GRCh38
NC_000023.10:g.154197765_154197766delinsCA , CM000685.1:g.154197765_154197766delinsCA GRCh37
NC_000023.9:g.153850959_153850960delinsCA NCBI36
NG_011403.1:g.58233_58234delinsTG
NG_011403.2:g.58233_58234delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.849_850delinsTG MANE Select ENSP00000353393.4:p.Pro283=
ENST00000647125.1:c.*725_*726delinsTG ENSP00000496062.1:n.*725_*726delinsTG
ENST00000360256.8:c.849_850delinsTG ENSP00000353393.4:p.Pro283=
NM_000132.3:c.849_850delinsTG NP_000123.1:p.Pro283=
XM_011531126.1:c.744_745delinsTG XP_011529428.1:p.Pro248=
NM_000132.4:c.849_850delinsTG MANE Select NP_000123.1:p.Pro283=
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