Canonical Allele Identifier: CA2623810416

Gene: F7

Linked Data

• gnomAD v4: 13-113119458-TGC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113119459_113119460del , CM000675.2:g.113119459_113119460del	GRCh38
NC_000013.10:g.113773773_113773774del , CM000675.1:g.113773773_113773774del	GRCh37
NC_000013.9:g.112821774_112821775del	NCBI36
NG_009258.1:g.1661_1662del , LRG_548:g.1661_1662del
NG_009262.1:g.18669_18670del , LRG_554:g.18669_18670del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.*451_*452del MANE Select	ENSP00000329546.4:n.*451_*452del
ENST00000346342.7:c.*451_*452del	ENSP00000329546.3:n.*451_*452del
ENST00000375581.3:c.*451_*452del	ENSP00000364731.3:n.*451_*452del
ENST00000541084.5:c.*451_*452del	ENSP00000442051.2:n.*451_*452del
NM_000131.4:c.*451_*452del , LRG_554t1:c.*451_*452del	NP_000122.1:n.*451_*452del
NM_001267554.1:c.*451_*452del	NP_001254483.1:n.*451_*452del
NM_019616.3:c.*451_*452del , LRG_554t2:c.*451_*452del	NP_062562.1:n.*451_*452del
NR_051961.1:n.1873_1874del
XM_006719963.2:c.*451_*452del	XP_006720026.1:n.*451_*452del
XM_011537474.1:c.*451_*452del	XP_011535776.1:n.*451_*452del
XM_011537475.1:c.*451_*452del	XP_011535777.1:n.*451_*452del
XM_011537476.1:c.*451_*452del	XP_011535778.1:n.*451_*452del
XM_011537477.1:c.*451_*452del	XP_011535779.1:n.*451_*452del
XM_006719963.3:c.*451_*452del	XP_006720026.2:n.*451_*452del
XM_011537474.2:c.*451_*452del	XP_011535776.2:n.*451_*452del
XM_011537475.2:c.*451_*452del	XP_011535777.2:n.*451_*452del
XM_011537476.2:c.*451_*452del	XP_011535778.1:n.*451_*452del
NM_019616.4:c.*451_*452del MANE Select	NP_062562.1:n.*451_*452del
NR_051961.2:n.1870_1871del
NM_001267554.2:c.*451_*452del	NP_001254483.1:n.*451_*452del