Canonical Allele Identifier: CA2575461624

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113114054T>A , CM000675.2:g.113114054T>A	GRCh38
NC_000013.10:g.113768368T>A , CM000675.1:g.113768368T>A	GRCh37
NC_000013.9:g.112816369T>A	NCBI36
NG_009262.1:g.13264T>A , LRG_554:g.13264T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.364+94T>A MANE Select	ENSP00000329546.4:n.364+94T>A
ENST00000346342.7:c.364+94T>A	ENSP00000329546.3:n.364+94T>A
ENST00000375581.3:c.430+94T>A	ENSP00000364731.3:n.430+94T>A
ENST00000444337.1:c.*172+94T>A	ENSP00000387669.1:n.*172+94T>A
ENST00000473085.1:n.311+94T>A
ENST00000479674.1:n.697+94T>A
ENST00000541084.5:c.178+94T>A	ENSP00000442051.2:n.178+94T>A
NM_000131.4:c.430+94T>A , LRG_554t1:c.430+94T>A	NP_000122.1:n.430+94T>A
NM_001267554.1:c.178+94T>A	NP_001254483.1:n.178+94T>A
NM_019616.3:c.364+94T>A , LRG_554t2:c.364+94T>A	NP_062562.1:n.364+94T>A
NR_051961.1:n.451+94T>A
XM_006719963.2:c.364+94T>A	XP_006720026.1:n.364+94T>A
XM_011537474.1:c.364+94T>A	XP_011535776.1:n.364+94T>A
XM_011537475.1:c.178+94T>A	XP_011535777.1:n.178+94T>A
XM_011537477.1:c.325+94T>A	XP_011535779.1:n.325+94T>A
XM_006719963.3:c.409+94T>A	XP_006720026.2:n.409+94T>A
XM_011537474.2:c.409+94T>A	XP_011535776.2:n.409+94T>A
XM_011537475.2:c.223+94T>A	XP_011535777.2:n.223+94T>A
XM_011537476.2:c.-715T>A	XP_011535778.1:n.-715T>A
NM_019616.4:c.364+94T>A MANE Select	NP_062562.1:n.364+94T>A
NR_051961.2:n.448+94T>A
NM_001267554.2:c.178+94T>A	NP_001254483.1:n.178+94T>A