Canonical Allele Identifier: CA2466807371
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154837499_154837502delinsGATT , CM000685.2:g.154837499_154837502delinsGATT GRCh38
NC_000023.10:g.154065774_154065777delinsGATT , CM000685.1:g.154065774_154065777delinsGATT GRCh37
NC_000023.9:g.153718968_153718971delinsGATT NCBI36
NG_011403.1:g.190222_190225delinsAATC
NG_033065.1:g.2161_2164delinsAATC
NG_011403.2:g.190222_190225delinsAATC

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.*95_*98delinsAATC MANE Select ENSP00000353393.4:n.*95_*98delinsAATC
ENST00000644698.1:c.*95_*98delinsAATC ENSP00000495706.1:n.*95_*98delinsAATC
ENST00000330287.10:c.*95_*98delinsAATC ENSP00000327895.6:n.*95_*98delinsAATC
ENST00000360256.8:c.*95_*98delinsAATC ENSP00000353393.4:n.*95_*98delinsAATC
NM_000132.3:c.*95_*98delinsAATC NP_000123.1:n.*95_*98delinsAATC
NM_019863.2:c.*95_*98delinsAATC NP_063916.1:n.*95_*98delinsAATC
XM_011531126.1:c.*95_*98delinsAATC XP_011529428.1:n.*95_*98delinsAATC
NM_000132.4:c.*95_*98delinsAATC MANE Select NP_000123.1:n.*95_*98delinsAATC
NM_019863.3:c.*95_*98delinsAATC NP_063916.1:n.*95_*98delinsAATC