Canonical Allele Identifier: CA695269007

Gene: F7

Linked Data

• dbSNP Id: rs1197354817
• gnomAD v3: 13-113119118-G-GTTA
• gnomAD v4: 13-113119118-G-GTTA
• MyVariant Identifiers: chr13:g.113773432_113773433insTTA (hg19) ; chr13:g.113119118_113119119insTTA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113119118_113119119insTTA , CM000675.2:g.113119118_113119119insTTA	GRCh38
NC_000013.10:g.113773432_113773433insTTA , CM000675.1:g.113773432_113773433insTTA	GRCh37
NC_000013.9:g.112821433_112821434insTTA	NCBI36
NG_009258.1:g.1320_1321insTTA , LRG_548:g.1320_1321insTTA
NG_009262.1:g.18328_18329insTTA , LRG_554:g.18328_18329insTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.*110_*111insTTA MANE Select	ENSP00000329546.4:n.*110_*111insTTA
ENST00000346342.7:c.*110_*111insTTA	ENSP00000329546.3:n.*110_*111insTTA
ENST00000375581.3:c.*110_*111insTTA	ENSP00000364731.3:n.*110_*111insTTA
ENST00000541084.5:c.*110_*111insTTA	ENSP00000442051.2:n.*110_*111insTTA
NM_000131.4:c.*110_*111insTTA , LRG_554t1:c.*110_*111insTTA	NP_000122.1:n.*110_*111insTTA
NM_001267554.1:c.*110_*111insTTA	NP_001254483.1:n.*110_*111insTTA
NM_019616.3:c.*110_*111insTTA , LRG_554t2:c.*110_*111insTTA	NP_062562.1:n.*110_*111insTTA
NR_051961.1:n.1532_1533insTTA
XM_006719963.2:c.*110_*111insTTA	XP_006720026.1:n.*110_*111insTTA
XM_011537474.1:c.*110_*111insTTA	XP_011535776.1:n.*110_*111insTTA
XM_011537475.1:c.*110_*111insTTA	XP_011535777.1:n.*110_*111insTTA
XM_011537476.1:c.*110_*111insTTA	XP_011535778.1:n.*110_*111insTTA
XM_011537477.1:c.*110_*111insTTA	XP_011535779.1:n.*110_*111insTTA
XM_006719963.3:c.*110_*111insTTA	XP_006720026.2:n.*110_*111insTTA
XM_011537474.2:c.*110_*111insTTA	XP_011535776.2:n.*110_*111insTTA
XM_011537475.2:c.*110_*111insTTA	XP_011535777.2:n.*110_*111insTTA
XM_011537476.2:c.*110_*111insTTA	XP_011535778.1:n.*110_*111insTTA
NM_019616.4:c.*110_*111insTTA MANE Select	NP_062562.1:n.*110_*111insTTA
NR_051961.2:n.1529_1530insTTA
NM_001267554.2:c.*110_*111insTTA	NP_001254483.1:n.*110_*111insTTA