Canonical Allele Identifier: CA2695238484
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154997030_154997031delinsTA , CM000685.2:g.154997030_154997031delinsTA GRCh38
NC_000023.10:g.154225305_154225306delinsTA , CM000685.1:g.154225305_154225306delinsTA GRCh37
NC_000023.9:g.153878499_153878500delinsTA NCBI36
NG_011403.1:g.30693_30694delinsTA
NG_011403.2:g.30693_30694delinsTA

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.330_331delinsTA MANE Select ENSP00000353393.4:p.Met110_Ala111delinsIl...
ENST00000647125.1:c.*116_*117delinsTA ENSP00000496062.1:n.*116_*117delinsTA
ENST00000360256.8:c.330_331delinsTA ENSP00000353393.4:p.Met110_Ala111delinsIl...
ENST00000423959.5:c.225_226delinsTA ENSP00000409446.1:p.Met75_Ala76delinsIleT...
ENST00000453950.1:c.312_313delinsTA ENSP00000389153.1:p.Met104_Ala105delinsIl...
NM_000132.3:c.330_331delinsTA NP_000123.1:p.Met110_Ala111delinsIleThr
XM_011531126.1:c.225_226delinsTA XP_011529428.1:p.Met75_Ala76delinsIleThr
NM_000132.4:c.330_331delinsTA MANE Select NP_000123.1:p.Met110_Ala111delinsIleThr