Canonical Allele Identifier: CA612690897

Gene: F7

Linked Data

• dbSNP Id: rs1056452548
• gnomAD v2: 13-113773811-GCA-G
• gnomAD v3: 13-113119497-GCA-G
• gnomAD v4: 13-113119497-GCA-G
• MyVariant Identifiers: chr13:g.113773814_113773815del (hg19) ; chr13:g.113773812_113773813del (hg19) ; chr13:g.113119500_113119501del (hg38) ; chr13:g.113119498_113119499del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113119505_113119506del , CM000675.2:g.113119505_113119506del	GRCh38
NC_000013.10:g.113773819_113773820del , CM000675.1:g.113773819_113773820del	GRCh37
NC_000013.9:g.112821820_112821821del	NCBI36
NG_009258.1:g.1707_1708del , LRG_548:g.1707_1708del
NG_009262.1:g.18715_18716del , LRG_554:g.18715_18716del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.*497_*498del MANE Select	ENSP00000329546.4:n.*497_*498del
ENST00000346342.7:c.*497_*498del	ENSP00000329546.3:n.*497_*498del
ENST00000375581.3:c.*497_*498del	ENSP00000364731.3:n.*497_*498del
ENST00000541084.5:c.*497_*498del	ENSP00000442051.2:n.*497_*498del
NM_000131.4:c.*497_*498del , LRG_554t1:c.*497_*498del	NP_000122.1:n.*497_*498del
NM_001267554.1:c.*497_*498del	NP_001254483.1:n.*497_*498del
NM_019616.3:c.*497_*498del , LRG_554t2:c.*497_*498del	NP_062562.1:n.*497_*498del
NR_051961.1:n.1919_1920del
XM_006719963.2:c.*497_*498del	XP_006720026.1:n.*497_*498del
XM_011537474.1:c.*497_*498del	XP_011535776.1:n.*497_*498del
XM_011537475.1:c.*497_*498del	XP_011535777.1:n.*497_*498del
XM_011537476.1:c.*497_*498del	XP_011535778.1:n.*497_*498del
XM_011537477.1:c.*497_*498del	XP_011535779.1:n.*497_*498del
XM_006719963.3:c.*497_*498del	XP_006720026.2:n.*497_*498del
XM_011537474.2:c.*497_*498del	XP_011535776.2:n.*497_*498del
XM_011537475.2:c.*497_*498del	XP_011535777.2:n.*497_*498del
XM_011537476.2:c.*497_*498del	XP_011535778.1:n.*497_*498del
NM_019616.4:c.*497_*498del MANE Select	NP_062562.1:n.*497_*498del
NR_051961.2:n.1916_1917del
NM_001267554.2:c.*497_*498del	NP_001254483.1:n.*497_*498del