Canonical Allele Identifier: CA2466828178

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154904029_154904030delinsTC , CM000685.2:g.154904029_154904030delinsTC	GRCh38
NC_000023.10:g.154132304_154132305delinsTC , CM000685.1:g.154132304_154132305delinsTC	GRCh37
NC_000023.9:g.153785498_153785499delinsTC	NCBI36
NG_011403.1:g.123694_123695delinsGA
NG_011403.2:g.123694_123695delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5874_5875delinsGA MANE Select	ENSP00000353393.4:p.Arg1958=
ENST00000360256.8:c.5874_5875delinsGA	ENSP00000353393.4:p.Arg1958=
NM_000132.3:c.5874_5875delinsGA	NP_000123.1:p.Arg1958=
XM_011531126.1:c.5769_5770delinsGA	XP_011529428.1:p.Arg1923=
NM_000132.4:c.5874_5875delinsGA MANE Select	NP_000123.1:p.Arg1958=