Canonical Allele Identifier: CA2623809970

Gene: F10

Linked Data

• gnomAD v4: 13-113149296-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149297del , CM000675.2:g.113149297del	GRCh38
NC_000013.10:g.113803611del , CM000675.1:g.113803611del	GRCh37
NC_000013.9:g.112851612del	NCBI36
NG_009258.1:g.31499del , LRG_548:g.31499del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.1247del MANE Select	ENSP00000364709.3:p.Gln416ArgfsTer18
ENST00000375551.7:c.*238del	ENSP00000364701.3:n.*238del
ENST00000375559.7:c.1247del	ENSP00000364709.3:p.Gln416ArgfsTer18
ENST00000409306.5:c.*238del	ENSP00000387092.1:n.*238del
NM_000504.3:c.1247del , LRG_548t1:c.1247del	NP_000495.1:p.Gln416ArgfsTer18
NM_001312674.1:c.1115del	NP_001299603.1:p.Gln372ArgfsTer18
NM_001312675.1:c.*238del	NP_001299604.1:n.*238del
NM_000504.4:c.1247del MANE Select	NP_000495.1:p.Gln416ArgfsTer18
NM_001312674.2:c.1115del	NP_001299603.1:p.Gln372ArgfsTer18
NM_001312675.2:c.*238del	NP_001299604.1:n.*238del