Canonical Allele Identifier: CA645237042

Gene: F8

Linked Data

• dbSNP Id: rs1557270999
• gnomAD v2: X-154065762-AGTGTCT-A
• gnomAD v3: X-154837487-AGTGTCT-A
• gnomAD v4: X-154837487-AGTGTCT-A
• MyVariant Identifiers: chrX:g.154065763_154065768del (hg19) ; chrX:g.154837488_154837493del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837489_154837494del , CM000685.2:g.154837489_154837494del	GRCh38
NC_000023.10:g.154065764_154065769del , CM000685.1:g.154065764_154065769del	GRCh37
NC_000023.9:g.153718958_153718963del	NCBI36
NG_011403.1:g.190231_190236del
NG_033065.1:g.2170_2175del
NG_011403.2:g.190231_190236del

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.*104_*109del MANE Select	ENSP00000353393.4:n.*104_*109del
ENST00000644698.1:c.*104_*109del	ENSP00000495706.1:n.*104_*109del
ENST00000330287.10:c.*104_*109del	ENSP00000327895.6:n.*104_*109del
ENST00000360256.8:c.*104_*109del	ENSP00000353393.4:n.*104_*109del
NM_000132.3:c.*104_*109del	NP_000123.1:n.*104_*109del
NM_019863.2:c.*104_*109del	NP_063916.1:n.*104_*109del
XM_011531126.1:c.*104_*109del	XP_011529428.1:n.*104_*109del
NM_000132.4:c.*104_*109del MANE Select	NP_000123.1:n.*104_*109del
NM_019863.3:c.*104_*109del	NP_063916.1:n.*104_*109del