Canonical Allele Identifier: CA2695237115

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837725_154837726delinsAAATC , CM000685.2:g.154837725_154837726delinsAAATC	GRCh38
NC_000023.10:g.154066000_154066001delinsAAATC , CM000685.1:g.154066000_154066001delinsAAATC	GRCh37
NC_000023.9:g.153719194_153719195delinsAAATC	NCBI36
NG_011403.1:g.189998_189999delinsGATTT
NG_033065.1:g.1937_1938delinsGATTT
NG_011403.2:g.189998_189999delinsGATTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6927_6928delinsGATTT MANE Select	ENSP00000353393.4:p.Phe2309_Thr2310delinsLeuIleSer
ENST00000644698.1:c.660_661delinsGATTT	ENSP00000495706.1:p.Phe220_Thr221delinsLeuIleSer
ENST00000330287.10:c.522_523delinsGATTT	ENSP00000327895.6:p.Phe174_Thr175delinsLeuIleSer
ENST00000360256.8:c.6927_6928delinsGATTT	ENSP00000353393.4:p.Phe2309_Thr2310delinsLeuIleSer
NM_000132.3:c.6927_6928delinsGATTT	NP_000123.1:p.Phe2309_Thr2310delinsLeuIleSer
NM_019863.2:c.522_523delinsGATTT	NP_063916.1:p.Phe174_Thr175delinsLeuIleSer
XM_011531126.1:c.6822_6823delinsGATTT	XP_011529428.1:p.Phe2274_Thr2275delinsLeuIleSer
NM_000132.4:c.6927_6928delinsGATTT MANE Select	NP_000123.1:p.Phe2309_Thr2310delinsLeuIleSer
NM_019863.3:c.522_523delinsGATTT	NP_063916.1:p.Phe174_Thr175delinsLeuIleSer