Canonical Allele Identifier: CA2579744054

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837561_154837562del , CM000685.2:g.154837561_154837562del	GRCh38
NC_000023.10:g.154065836_154065837del , CM000685.1:g.154065836_154065837del	GRCh37
NC_000023.9:g.153719030_153719031del	NCBI36
NG_011403.1:g.190165_190166del
NG_033065.1:g.2104_2105del
NG_011403.2:g.190165_190166del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.*38_*39del MANE Select	ENSP00000353393.4:n.*38_*39del
ENST00000644698.1:c.*38_*39del	ENSP00000495706.1:n.*38_*39del
ENST00000330287.10:c.*38_*39del	ENSP00000327895.6:n.*38_*39del
ENST00000360256.8:c.*38_*39del	ENSP00000353393.4:n.*38_*39del
NM_000132.3:c.*38_*39del	NP_000123.1:n.*38_*39del
NM_019863.2:c.*38_*39del	NP_063916.1:n.*38_*39del
XM_011531126.1:c.*38_*39del	XP_011529428.1:n.*38_*39del
NM_000132.4:c.*38_*39del MANE Select	NP_000123.1:n.*38_*39del
NM_019863.3:c.*38_*39del	NP_063916.1:n.*38_*39del