Canonical Allele Identifier: CA2466828141
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154903939_154903944delinsCCTCTT , CM000685.2:g.154903939_154903944delinsCCTCTT GRCh38
NC_000023.10:g.154132214_154132219delinsCCTCTT , CM000685.1:g.154132214_154132219delinsCCTCTT GRCh37
NC_000023.9:g.153785408_153785413delinsCCTCTT NCBI36
NG_011403.1:g.123780_123785delinsAAGAGG
NG_011403.2:g.123780_123785delinsAAGAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5960_5965delinsAAGAGG MANE Select ENSP00000353393.4:p.Lys1987=
ENST00000360256.8:c.5960_5965delinsAAGAGG ENSP00000353393.4:p.Lys1987=
NM_000132.3:c.5960_5965delinsAAGAGG NP_000123.1:p.Lys1987=
XM_011531126.1:c.5855_5860delinsAAGAGG XP_011529428.1:p.Lys1952=
NM_000132.4:c.5960_5965delinsAAGAGG MANE Select NP_000123.1:p.Lys1987=
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