Canonical Allele Identifier: CA1008977102

Gene: F5

Linked Data

• gnomAD v3: 1-169549634-CAAAAA-C
• gnomAD v4: 1-169549634-CAAAAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169549643_169549647del , CM000663.2:g.169549643_169549647del	GRCh38
NC_000001.10:g.169518881_169518885del , CM000663.1:g.169518881_169518885del	GRCh37
NC_000001.9:g.167785505_167785509del	NCBI36
NG_011806.1:g.41893_41897del , LRG_553:g.41893_41897del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.1611+162_1611+166del MANE Select	ENSP00000356771.3:n.1611+162_1611+166del
ENST00000367796.3:c.1611+162_1611+166del	ENSP00000356770.3:n.1611+162_1611+166del
ENST00000367797.7:c.1611+162_1611+166del	ENSP00000356771.3:n.1611+162_1611+166del
NM_000130.4:c.1611+162_1611+166del , LRG_553t1:c.1611+162_1611+166del	NP_000121.2:n.1611+162_1611+166del
XM_017000660.2:c.1200+162_1200+166del	XP_016856149.1:n.1200+162_1200+166del
NM_000130.5:c.1611+162_1611+166del MANE Select	NP_000121.2:n.1611+162_1611+166del