Canonical Allele Identifier: CA2623810653

Gene: F7

Linked Data

• gnomAD v4: 13-113119523-G-GTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113119523_113119524insTTT , CM000675.2:g.113119523_113119524insTTT	GRCh38
NC_000013.10:g.113773837_113773838insTTT , CM000675.1:g.113773837_113773838insTTT	GRCh37
NC_000013.9:g.112821838_112821839insTTT	NCBI36
NG_009258.1:g.1725_1726insTTT , LRG_548:g.1725_1726insTTT
NG_009262.1:g.18733_18734insTTT , LRG_554:g.18733_18734insTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.*515_*516insTTT MANE Select	ENSP00000329546.4:n.*515_*516insTTT
ENST00000346342.7:c.*515_*516insTTT	ENSP00000329546.3:n.*515_*516insTTT
ENST00000375581.3:c.*515_*516insTTT	ENSP00000364731.3:n.*515_*516insTTT
ENST00000541084.5:c.*515_*516insTTT	ENSP00000442051.2:n.*515_*516insTTT
NM_000131.4:c.*515_*516insTTT , LRG_554t1:c.*515_*516insTTT	NP_000122.1:n.*515_*516insTTT
NM_001267554.1:c.*515_*516insTTT	NP_001254483.1:n.*515_*516insTTT
NM_019616.3:c.*515_*516insTTT , LRG_554t2:c.*515_*516insTTT	NP_062562.1:n.*515_*516insTTT
NR_051961.1:n.1937_1938insTTT
XM_006719963.2:c.*515_*516insTTT	XP_006720026.1:n.*515_*516insTTT
XM_011537474.1:c.*515_*516insTTT	XP_011535776.1:n.*515_*516insTTT
XM_011537475.1:c.*515_*516insTTT	XP_011535777.1:n.*515_*516insTTT
XM_011537476.1:c.*515_*516insTTT	XP_011535778.1:n.*515_*516insTTT
XM_011537477.1:c.*515_*516insTTT	XP_011535779.1:n.*515_*516insTTT
XM_006719963.3:c.*515_*516insTTT	XP_006720026.2:n.*515_*516insTTT
XM_011537474.2:c.*515_*516insTTT	XP_011535776.2:n.*515_*516insTTT
XM_011537475.2:c.*515_*516insTTT	XP_011535777.2:n.*515_*516insTTT
XM_011537476.2:c.*515_*516insTTT	XP_011535778.1:n.*515_*516insTTT
NM_019616.4:c.*515_*516insTTT MANE Select	NP_062562.1:n.*515_*516insTTT
NR_051961.2:n.1934_1935insTTT
NM_001267554.2:c.*515_*516insTTT	NP_001254483.1:n.*515_*516insTTT