Canonical Allele Identifier: CA1206149174

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169555147_169555153delinsACCTTTG , CM000663.2:g.169555147_169555153delinsACCTTTG	GRCh38
NC_000001.10:g.169524385_169524391delinsACCTTTG , CM000663.1:g.169524385_169524391delinsACCTTTG	GRCh37
NC_000001.9:g.167791009_167791015delinsACCTTTG	NCBI36
NG_011806.1:g.36379_36385delinsCAAAGGT , LRG_553:g.36379_36385delinsCAAAGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.1118+29_1118+35delinsCAAAGGT MANE Select	ENSP00000356771.3:n.1118+29_1118+35delinsCAAAGGT
ENST00000367796.3:c.1118+29_1118+35delinsCAAAGGT	ENSP00000356770.3:n.1118+29_1118+35delinsCAAAGGT
ENST00000367797.7:c.1118+29_1118+35delinsCAAAGGT	ENSP00000356771.3:n.1118+29_1118+35delinsCAAAGGT
NM_000130.4:c.1118+29_1118+35delinsCAAAGGT , LRG_553t1:c.1118+29_1118+35delinsCAAAGGT	NP_000121.2:n.1118+29_1118+35delinsCAAAGGT
XM_017000660.2:c.707+29_707+35delinsCAAAGGT	XP_016856149.1:n.707+29_707+35delinsCAAAGGT
NM_000130.5:c.1118+29_1118+35delinsCAAAGGT MANE Select	NP_000121.2:n.1118+29_1118+35delinsCAAAGGT