Canonical Allele Identifier: CA2695169147

Gene: F8

Linked Data

• gnomAD v4: X-154956892-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154956893del , CM000685.2:g.154956893del	GRCh38
NC_000023.10:g.154185168del , CM000685.1:g.154185168del	GRCh37
NC_000023.9:g.153838362del	NCBI36
NG_011403.1:g.70831del
NG_011403.2:g.70831del

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.1752+64del MANE Select	ENSP00000353393.4:n.1752+64del
ENST00000647125.1:c.*1628+64del	ENSP00000496062.1:n.*1628+64del
ENST00000360256.8:c.1752+64del	ENSP00000353393.4:n.1752+64del
NM_000132.3:c.1752+64del	NP_000123.1:n.1752+64del
XM_011531126.1:c.1647+64del	XP_011529428.1:n.1647+64del
NM_000132.4:c.1752+64del MANE Select	NP_000123.1:n.1752+64del