Canonical Allele Identifier: CA7059829

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113106842C>T , CM000675.2:g.113106842C>T	GRCh38
NC_000013.10:g.113761156C>T , CM000675.1:g.113761156C>T	GRCh37
NC_000013.9:g.112809157C>T	NCBI36
NG_009262.1:g.6052C>T , LRG_554:g.6052C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_019616.4:c.64+937C>T MANE Select	NP_062562.1:n.64+937C>T
ENST00000346342.8:c.64+937C>T MANE Select	ENSP00000329546.4:n.64+937C>T
NM_000131.4:c.65-3C>T , LRG_554t1:c.65-3C>T	NP_000122.1:n.65-3C>T
NM_001267554.1:c.64+937C>T	NP_001254483.1:n.64+937C>T
NM_001267554.2:c.64+937C>T	NP_001254483.1:n.64+937C>T
NM_019616.3:c.64+937C>T , LRG_554t2:c.64+937C>T	NP_062562.1:n.64+937C>T
NR_051961.1:n.118+937C>T
NR_051961.2:n.115+937C>T
ENST00000346342.7:c.64+937C>T	ENSP00000329546.3:n.64+937C>T
ENST00000375581.3:c.65-3C>T	ENSP00000364731.3:n.65-3C>T
ENST00000444337.1:c.64+937C>T	ENSP00000387669.1:n.64+937C>T
ENST00000541084.5:c.64+937C>T	ENSP00000442051.2:n.64+937C>T
XM_006719963.2:c.64+937C>T	XP_006720026.1:n.64+937C>T
XM_006719963.3:c.109+937C>T	XP_006720026.2:n.109+937C>T
XM_011537474.1:c.64+937C>T	XP_011535776.1:n.64+937C>T
XM_011537474.2:c.109+937C>T	XP_011535776.2:n.109+937C>T
XM_011537475.1:c.64+937C>T	XP_011535777.1:n.64+937C>T
XM_011537475.2:c.109+937C>T	XP_011535777.2:n.109+937C>T
XM_011537477.1:c.64+937C>T	XP_011535779.1:n.64+937C>T