Canonical Allele Identifier: CA2695237247

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154956953_154956954insAACCT , CM000685.2:g.154956953_154956954insAACCT	GRCh38
NC_000023.10:g.154185228_154185229insAACCT , CM000685.1:g.154185228_154185229insAACCT	GRCh37
NC_000023.9:g.153838422_153838423insAACCT	NCBI36
NG_011403.1:g.70772_70773insGTTAG
NG_011403.2:g.70772_70773insGTTAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.1752+5_1752+6insGTTAG MANE Select	ENSP00000353393.4:n.1752+5_1752+6insGTTAG
ENST00000647125.1:c.*1628+5_*1628+6insGTTAG	ENSP00000496062.1:n.*1628+5_*1628+6insGTTAG
ENST00000360256.8:c.1752+5_1752+6insGTTAG	ENSP00000353393.4:n.1752+5_1752+6insGTTAG
NM_000132.3:c.1752+5_1752+6insGTTAG	NP_000123.1:n.1752+5_1752+6insGTTAG
XM_011531126.1:c.1647+5_1647+6insGTTAG	XP_011529428.1:n.1647+5_1647+6insGTTAG
NM_000132.4:c.1752+5_1752+6insGTTAG MANE Select	NP_000123.1:n.1752+5_1752+6insGTTAG