Canonical Allele Identifier: CA2695237107

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837664_154837665del , CM000685.2:g.154837664_154837665del	GRCh38
NC_000023.10:g.154065939_154065940del , CM000685.1:g.154065939_154065940del	GRCh37
NC_000023.9:g.153719133_153719134del	NCBI36
NG_011403.1:g.190059_190060del
NG_033065.1:g.1998_1999del
NG_011403.2:g.190059_190060del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6988_6989del MANE Select	ENSP00000353393.4:p.Gln2330GlufsTer?
ENST00000644698.1:c.721_722del	ENSP00000495706.1:p.Gln241GlufsTer?
ENST00000330287.10:c.583_584del	ENSP00000327895.6:p.Gln195GlufsTer?
ENST00000360256.8:c.6988_6989del	ENSP00000353393.4:p.Gln2330GlufsTer?
NM_000132.3:c.6988_6989del	NP_000123.1:p.Gln2330GlufsTer?
NM_019863.2:c.583_584del	NP_063916.1:p.Gln195GlufsTer?
XM_011531126.1:c.6883_6884del	XP_011529428.1:p.Gln2295GlufsTer?
NM_000132.4:c.6988_6989del MANE Select	NP_000123.1:p.Gln2330GlufsTer?
NM_019863.3:c.583_584del	NP_063916.1:p.Gln195GlufsTer?