Canonical Allele Identifier: CA2623810422

Gene: F7

Linked Data

• gnomAD v4: 13-113119459-G-GTA

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113119459_113119460insTA , CM000675.2:g.113119459_113119460insTA	GRCh38
NC_000013.10:g.113773773_113773774insTA , CM000675.1:g.113773773_113773774insTA	GRCh37
NC_000013.9:g.112821774_112821775insTA	NCBI36
NG_009258.1:g.1661_1662insTA , LRG_548:g.1661_1662insTA
NG_009262.1:g.18669_18670insTA , LRG_554:g.18669_18670insTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.*451_*452insTA MANE Select	ENSP00000329546.4:n.*451_*452insTA
ENST00000346342.7:c.*451_*452insTA	ENSP00000329546.3:n.*451_*452insTA
ENST00000375581.3:c.*451_*452insTA	ENSP00000364731.3:n.*451_*452insTA
ENST00000541084.5:c.*451_*452insTA	ENSP00000442051.2:n.*451_*452insTA
NM_000131.4:c.*451_*452insTA , LRG_554t1:c.*451_*452insTA	NP_000122.1:n.*451_*452insTA
NM_001267554.1:c.*451_*452insTA	NP_001254483.1:n.*451_*452insTA
NM_019616.3:c.*451_*452insTA , LRG_554t2:c.*451_*452insTA	NP_062562.1:n.*451_*452insTA
NR_051961.1:n.1873_1874insTA
XM_006719963.2:c.*451_*452insTA	XP_006720026.1:n.*451_*452insTA
XM_011537474.1:c.*451_*452insTA	XP_011535776.1:n.*451_*452insTA
XM_011537475.1:c.*451_*452insTA	XP_011535777.1:n.*451_*452insTA
XM_011537476.1:c.*451_*452insTA	XP_011535778.1:n.*451_*452insTA
XM_011537477.1:c.*451_*452insTA	XP_011535779.1:n.*451_*452insTA
XM_006719963.3:c.*451_*452insTA	XP_006720026.2:n.*451_*452insTA
XM_011537474.2:c.*451_*452insTA	XP_011535776.2:n.*451_*452insTA
XM_011537475.2:c.*451_*452insTA	XP_011535777.2:n.*451_*452insTA
XM_011537476.2:c.*451_*452insTA	XP_011535778.1:n.*451_*452insTA
NM_019616.4:c.*451_*452insTA MANE Select	NP_062562.1:n.*451_*452insTA
NR_051961.2:n.1870_1871insTA
NM_001267554.2:c.*451_*452insTA	NP_001254483.1:n.*451_*452insTA