Canonical Allele Identifier: CA2695237116

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837734_154837735del , CM000685.2:g.154837734_154837735del	GRCh38
NC_000023.10:g.154066009_154066010del , CM000685.1:g.154066009_154066010del	GRCh37
NC_000023.9:g.153719203_153719204del	NCBI36
NG_011403.1:g.189990_189991del
NG_033065.1:g.1929_1930del
NG_011403.2:g.189990_189991del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6919_6920del MANE Select	ENSP00000353393.4:p.Asp2307LeufsTer?
ENST00000644698.1:c.652_653del	ENSP00000495706.1:p.Asp218LeufsTer?
ENST00000330287.10:c.514_515del	ENSP00000327895.6:p.Asp172LeufsTer?
ENST00000360256.8:c.6919_6920del	ENSP00000353393.4:p.Asp2307LeufsTer?
NM_000132.3:c.6919_6920del	NP_000123.1:p.Asp2307LeufsTer?
NM_019863.2:c.514_515del	NP_063916.1:p.Asp172LeufsTer?
XM_011531126.1:c.6814_6815del	XP_011529428.1:p.Asp2272LeufsTer?
NM_000132.4:c.6919_6920del MANE Select	NP_000123.1:p.Asp2307LeufsTer?
NM_019863.3:c.514_515del	NP_063916.1:p.Asp172LeufsTer?