Canonical Allele Identifier: CA2695170496

Gene: F8

Linked Data

• gnomAD v4: X-155022621-CCAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.155022622_155022624del , CM000685.2:g.155022622_155022624del	GRCh38
NC_000023.10:g.154250897_154250899del , CM000685.1:g.154250897_154250899del	GRCh37
NC_000023.9:g.153904091_153904093del	NCBI36
NG_011403.1:g.5100_5102del
NG_011403.2:g.5100_5102del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.-72_-70del MANE Select	ENSP00000353393.4:n.-72_-70del
ENST00000647125.1:c.-72_-70del	ENSP00000496062.1:n.-72_-70del
ENST00000360256.8:c.-72_-70del	ENSP00000353393.4:n.-72_-70del
ENST00000423959.5:c.38+4156_38+4158del	ENSP00000409446.1:n.38+4156_38+4158del
ENST00000453950.1:c.39-128_39-126del	ENSP00000389153.1:n.39-128_39-126del
NM_000132.3:c.-72_-70del	NP_000123.1:n.-72_-70del
XM_011531126.1:c.38+4156_38+4158del	XP_011529428.1:n.38+4156_38+4158del
NM_000132.4:c.-72_-70del MANE Select	NP_000123.1:n.-72_-70del