Canonical Allele Identifier: CA1206147048

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169552764_169552770delinsACTTTCT , CM000663.2:g.169552764_169552770delinsACTTTCT	GRCh38
NC_000001.10:g.169522002_169522008delinsACTTTCT , CM000663.1:g.169522002_169522008delinsACTTTCT	GRCh37
NC_000001.9:g.167788626_167788632delinsACTTTCT	NCBI36
NG_011806.1:g.38762_38768delinsAGAAAGT , LRG_553:g.38762_38768delinsAGAAAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.1119-36_1119-30delinsAGAAAGT MANE Select	ENSP00000356771.3:n.1119-36_1119-30delinsAGAAAGT
ENST00000367796.3:c.1119-36_1119-30delinsAGAAAGT	ENSP00000356770.3:n.1119-36_1119-30delinsAGAAAGT
ENST00000367797.7:c.1119-36_1119-30delinsAGAAAGT	ENSP00000356771.3:n.1119-36_1119-30delinsAGAAAGT
NM_000130.4:c.1119-36_1119-30delinsAGAAAGT , LRG_553t1:c.1119-36_1119-30delinsAGAAAGT	NP_000121.2:n.1119-36_1119-30delinsAGAAAGT
XM_017000660.2:c.708-36_708-30delinsAGAAAGT	XP_016856149.1:n.708-36_708-30delinsAGAAAGT
NM_000130.5:c.1119-36_1119-30delinsAGAAAGT MANE Select	NP_000121.2:n.1119-36_1119-30delinsAGAAAGT