Canonical Allele Identifier: CA2695170485

Gene: F8

Linked Data

• gnomAD v4: X-155022560-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.155022561del , CM000685.2:g.155022561del	GRCh38
NC_000023.10:g.154250836del , CM000685.1:g.154250836del	GRCh37
NC_000023.9:g.153904030del	NCBI36
NG_011403.1:g.5163del
NG_011403.2:g.5163del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.-9del MANE Select	ENSP00000353393.4:n.-9del
ENST00000647125.1:c.-9del	ENSP00000496062.1:n.-9del
ENST00000360256.8:c.-9del	ENSP00000353393.4:n.-9del
ENST00000423959.5:c.38+4219del	ENSP00000409446.1:n.38+4219del
ENST00000453950.1:c.39-65del	ENSP00000389153.1:n.39-65del
NM_000132.3:c.-9del	NP_000123.1:n.-9del
XM_011531126.1:c.38+4219del	XP_011529428.1:n.38+4219del
NM_000132.4:c.-9del MANE Select	NP_000123.1:n.-9del