Canonical Allele Identifier: CA2512645791

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154953866_154953867insCA , CM000685.2:g.154953866_154953867insCA	GRCh38
NC_000023.10:g.154182141_154182142insCA , CM000685.1:g.154182141_154182142insCA	GRCh37
NC_000023.9:g.153835335_153835336insCA	NCBI36
NG_011403.1:g.73857_73858insTG
NG_011403.2:g.73857_73858insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.1903+25_1903+26insTG MANE Select	ENSP00000353393.4:n.1903+25_1903+26insTG
ENST00000647125.1:c.*1779+25_*1779+26insTG	ENSP00000496062.1:n.*1779+25_*1779+26insTG
ENST00000360256.8:c.1903+25_1903+26insTG	ENSP00000353393.4:n.1903+25_1903+26insTG
NM_000132.3:c.1903+25_1903+26insTG	NP_000123.1:n.1903+25_1903+26insTG
XM_011531126.1:c.1798+25_1798+26insTG	XP_011529428.1:n.1798+25_1798+26insTG
NM_000132.4:c.1903+25_1903+26insTG MANE Select	NP_000123.1:n.1903+25_1903+26insTG