Canonical Allele Identifier: CA2695238473

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154996969_154996972del , CM000685.2:g.154996969_154996972del	GRCh38
NC_000023.10:g.154225244_154225247del , CM000685.1:g.154225244_154225247del	GRCh37
NC_000023.9:g.153878438_153878441del	NCBI36
NG_011403.1:g.30754_30757del
NG_011403.2:g.30754_30757del

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.388+3_388+6del MANE Select	ENSP00000353393.4:n.388+3_388+6del
ENST00000647125.1:c.*174+3_*174+6del	ENSP00000496062.1:n.*174+3_*174+6del
ENST00000360256.8:c.388+3_388+6del	ENSP00000353393.4:n.388+3_388+6del
ENST00000423959.5:c.283+3_283+6del	ENSP00000409446.1:n.283+3_283+6del
ENST00000453950.1:c.370+3_370+6del	ENSP00000389153.1:n.370+3_370+6del
NM_000132.3:c.388+3_388+6del	NP_000123.1:n.388+3_388+6del
XM_011531126.1:c.283+3_283+6del	XP_011529428.1:n.283+3_283+6del
NM_000132.4:c.388+3_388+6del MANE Select	NP_000123.1:n.388+3_388+6del