Canonical Allele Identifier: CA2466865486

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.155022652_155022659delinsTAATGAAA , CM000685.2:g.155022652_155022659delinsTAATGAAA	GRCh38
NC_000023.10:g.154250927_154250934delinsTAATGAAA , CM000685.1:g.154250927_154250934delinsTAATGAAA	GRCh37
NC_000023.9:g.153904121_153904128delinsTAATGAAA	NCBI36
NG_011403.1:g.5065_5072delinsTTTCATTA
NG_011403.2:g.5065_5072delinsTTTCATTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.-107_-100delinsTTTCATTA MANE Select	ENSP00000353393.4:n.-107_-100delinsTTTCATTA
ENST00000647125.1:c.-107_-100delinsTTTCATTA	ENSP00000496062.1:n.-107_-100delinsTTTCATTA
ENST00000360256.8:c.-107_-100delinsTTTCATTA	ENSP00000353393.4:n.-107_-100delinsTTTCATTA
ENST00000423959.5:c.38+4121_38+4128delinsTTTCATTA	ENSP00000409446.1:n.38+4121_38+4128delinsTTTCATTA
ENST00000453950.1:c.39-163_39-156delinsTTTCATTA	ENSP00000389153.1:n.39-163_39-156delinsTTTCATTA
NM_000132.3:c.-107_-100delinsTTTCATTA	NP_000123.1:n.-107_-100delinsTTTCATTA
XM_011531126.1:c.38+4121_38+4128delinsTTTCATTA	XP_011529428.1:n.38+4121_38+4128delinsTTTCATTA
NM_000132.4:c.-107_-100delinsTTTCATTA MANE Select	NP_000123.1:n.-107_-100delinsTTTCATTA