Canonical Allele Identifier: CA645237043

Gene: F8

Linked Data

• dbSNP Id: rs1557271004
• gnomAD v2: X-154065771-T-TTGA
• gnomAD v3: X-154837496-T-TTGA
• gnomAD v4: X-154837496-T-TTGA
• MyVariant Identifiers: chrX:g.154065771_154065772insTGA (hg19) ; chrX:g.154837496_154837497insTGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837496_154837497insTGA , CM000685.2:g.154837496_154837497insTGA	GRCh38
NC_000023.10:g.154065771_154065772insTGA , CM000685.1:g.154065771_154065772insTGA	GRCh37
NC_000023.9:g.153718965_153718966insTGA	NCBI36
NG_011403.1:g.190227_190228insTCA
NG_033065.1:g.2166_2167insTCA
NG_011403.2:g.190227_190228insTCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.*100_*101insTCA MANE Select	ENSP00000353393.4:n.*100_*101insTCA
ENST00000644698.1:c.*100_*101insTCA	ENSP00000495706.1:n.*100_*101insTCA
ENST00000330287.10:c.*100_*101insTCA	ENSP00000327895.6:n.*100_*101insTCA
ENST00000360256.8:c.*100_*101insTCA	ENSP00000353393.4:n.*100_*101insTCA
NM_000132.3:c.*100_*101insTCA	NP_000123.1:n.*100_*101insTCA
NM_019863.2:c.*100_*101insTCA	NP_063916.1:n.*100_*101insTCA
XM_011531126.1:c.*100_*101insTCA	XP_011529428.1:n.*100_*101insTCA
NM_000132.4:c.*100_*101insTCA MANE Select	NP_000123.1:n.*100_*101insTCA
NM_019863.3:c.*100_*101insTCA	NP_063916.1:n.*100_*101insTCA