Canonical Allele Identifier: CA2513472588
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154837425_154837426insAGAT , CM000685.2:g.154837425_154837426insAGAT GRCh38
NC_000023.10:g.154065700_154065701insAGAT , CM000685.1:g.154065700_154065701insAGAT GRCh37
NC_000023.9:g.153718894_153718895insAGAT NCBI36
NG_011403.1:g.190298_190299insATCT
NG_033065.1:g.2237_2238insATCT
NG_011403.2:g.190298_190299insATCT

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.*171_*172insATCT MANE Select ENSP00000353393.4:n.*171_*172insATCT
ENST00000644698.1:c.*171_*172insATCT ENSP00000495706.1:n.*171_*172insATCT
ENST00000330287.10:c.*171_*172insATCT ENSP00000327895.6:n.*171_*172insATCT
ENST00000360256.8:c.*171_*172insATCT ENSP00000353393.4:n.*171_*172insATCT
NM_000132.3:c.*171_*172insATCT NP_000123.1:n.*171_*172insATCT
NM_019863.2:c.*171_*172insATCT NP_063916.1:n.*171_*172insATCT
XM_011531126.1:c.*171_*172insATCT XP_011529428.1:n.*171_*172insATCT
NM_000132.4:c.*171_*172insATCT MANE Select NP_000123.1:n.*171_*172insATCT
NM_019863.3:c.*171_*172insATCT NP_063916.1:n.*171_*172insATCT
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