Canonical Allele Identifier: CA2466815634

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154863131_154863134delinsTATA , CM000685.2:g.154863131_154863134delinsTATA	GRCh38
NC_000023.10:g.154091406_154091409delinsTATA , CM000685.1:g.154091406_154091409delinsTATA	GRCh37
NC_000023.9:g.153744600_153744603delinsTATA	NCBI36
NG_011403.1:g.164590_164593delinsTATA
NG_011403.2:g.164590_164593delinsTATA

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.6523_6526delinsTATA MANE Select	ENSP00000353393.4:p.Tyr2175=
ENST00000644698.1:c.256_259delinsTATA	ENSP00000495706.1:p.Tyr86=
ENST00000330287.10:c.118_121delinsTATA	ENSP00000327895.6:p.Tyr40=
ENST00000360256.8:c.6523_6526delinsTATA	ENSP00000353393.4:p.Tyr2175=
NM_000132.3:c.6523_6526delinsTATA	NP_000123.1:p.Tyr2175=
NM_019863.2:c.118_121delinsTATA	NP_063916.1:p.Tyr40=
XM_011531126.1:c.6418_6421delinsTATA	XP_011529428.1:p.Tyr2140=
NM_000132.4:c.6523_6526delinsTATA MANE Select	NP_000123.1:p.Tyr2175=
NM_019863.3:c.118_121delinsTATA	NP_063916.1:p.Tyr40=