Canonical Allele Identifier: CA645237044

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837500_154837502del , CM000685.2:g.154837500_154837502del	GRCh38
NC_000023.10:g.154065775_154065777del , CM000685.1:g.154065775_154065777del	GRCh37
NC_000023.9:g.153718969_153718971del	NCBI36
NG_011403.1:g.190222_190224del
NG_033065.1:g.2161_2163del
NG_011403.2:g.190222_190224del

Transcript Alleles

HGVS	Amino-acid Change
NM_000132.4:c.*95_*97del MANE Select	NP_000123.1:n.*95_*97del
ENST00000360256.9:c.*95_*97del MANE Select	ENSP00000353393.4:n.*95_*97del
NM_000132.3:c.*95_*97del	NP_000123.1:n.*95_*97del
NM_019863.2:c.*95_*97del	NP_063916.1:n.*95_*97del
NM_019863.3:c.*95_*97del	NP_063916.1:n.*95_*97del
ENST00000330287.10:c.*95_*97del	ENSP00000327895.6:n.*95_*97del
ENST00000360256.8:c.*95_*97del	ENSP00000353393.4:n.*95_*97del
ENST00000644698.1:c.*95_*97del	ENSP00000495706.1:n.*95_*97del
XM_011531126.1:c.*95_*97del	XP_011529428.1:n.*95_*97del