Canonical Allele Identifier: CA2695152087

Gene: F8

Linked Data

• gnomAD v4: X-154896309-A-ATGTG

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154896309_154896310insTGTG , CM000685.2:g.154896309_154896310insTGTG	GRCh38
NC_000023.10:g.154124584_154124585insTGTG , CM000685.1:g.154124584_154124585insTGTG	GRCh37
NC_000023.9:g.153777778_153777779insTGTG	NCBI36
NG_011403.1:g.131414_131415insCACA
NG_011403.2:g.131414_131415insCACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6274-78_6274-77insCACA MANE Select	ENSP00000353393.4:n.6274-78_6274-77insCACA
ENST00000360256.8:c.6274-78_6274-77insCACA	ENSP00000353393.4:n.6274-78_6274-77insCACA
NM_000132.3:c.6274-78_6274-77insCACA	NP_000123.1:n.6274-78_6274-77insCACA
XM_011531126.1:c.6169-78_6169-77insCACA	XP_011529428.1:n.6169-78_6169-77insCACA
NM_000132.4:c.6274-78_6274-77insCACA MANE Select	NP_000123.1:n.6274-78_6274-77insCACA