Canonical Allele Identifier: CA2575461723

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118352T>C , CM000675.2:g.113118352T>C	GRCh38
NC_000013.10:g.113772666T>C , CM000675.1:g.113772666T>C	GRCh37
NC_000013.9:g.112820667T>C	NCBI36
NG_009258.1:g.554T>C , LRG_548:g.554T>C
NG_009262.1:g.17562T>C , LRG_554:g.17562T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.740-61T>C MANE Select	ENSP00000329546.4:n.740-61T>C
ENST00000346342.7:c.740-61T>C	ENSP00000329546.3:n.740-61T>C
ENST00000375581.3:c.806-61T>C	ENSP00000364731.3:n.806-61T>C
ENST00000541084.5:c.554-61T>C	ENSP00000442051.2:n.554-61T>C
NM_000131.4:c.806-61T>C , LRG_554t1:c.806-61T>C	NP_000122.1:n.806-61T>C
NM_001267554.1:c.554-61T>C	NP_001254483.1:n.554-61T>C
NM_019616.3:c.740-61T>C , LRG_554t2:c.740-61T>C	NP_062562.1:n.740-61T>C
NR_051961.1:n.827-61T>C
XM_006719963.2:c.599-61T>C	XP_006720026.1:n.599-61T>C
XM_011537474.1:c.848-61T>C	XP_011535776.1:n.848-61T>C
XM_011537475.1:c.662-61T>C	XP_011535777.1:n.662-61T>C
XM_011537476.1:c.500-61T>C	XP_011535778.1:n.500-61T>C
XM_011537477.1:c.809-61T>C	XP_011535779.1:n.809-61T>C
XM_006719963.3:c.644-61T>C	XP_006720026.2:n.644-61T>C
XM_011537474.2:c.893-61T>C	XP_011535776.2:n.893-61T>C
XM_011537475.2:c.707-61T>C	XP_011535777.2:n.707-61T>C
XM_011537476.2:c.500-61T>C	XP_011535778.1:n.500-61T>C
NM_019616.4:c.740-61T>C MANE Select	NP_062562.1:n.740-61T>C
NR_051961.2:n.824-61T>C
NM_001267554.2:c.554-61T>C	NP_001254483.1:n.554-61T>C