Canonical Allele Identifier: CA595189261

Gene: FGF8

Linked Data

• dbSNP Id: rs1564631151
• gnomAD v2: 10-103531537-CG-C
• MyVariant Identifiers: chr10:g.103531538del (hg19) ; chr10:g.101771781del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771783del , CM000672.2:g.101771783del	GRCh38
NC_000010.10:g.103531540del , CM000672.1:g.103531540del	GRCh37
NC_000010.9:g.103521530del	NCBI36
NG_007151.1:g.9290del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.338-212del MANE Select	ENSP00000321797.2:n.338-212del
ENST00000618991.5:c.26-212del	ENSP00000484420.1:n.26-212del
ENST00000344255.8:c.305-212del	ENSP00000340039.3:n.305-212del
ENST00000320185.6:c.338-212del	ENSP00000321797.2:n.338-212del
ENST00000344255.7:c.305-212del	ENSP00000340039.3:n.305-212del
ENST00000346714.7:c.218-212del	ENSP00000344306.3:n.218-212del
ENST00000347978.2:c.251-212del	ENSP00000321945.2:n.251-212del
ENST00000469792.6:c.*302-212del	ENSP00000473299.1:n.*302-212del
ENST00000485728.1:n.214-212del
ENST00000618991.4:c.26-212del	ENSP00000484420.1:n.26-212del
NM_001206389.1:c.26-212del	NP_001193318.1:n.26-212del
NM_006119.4:c.251-212del	NP_006110.1:n.251-212del
NM_033163.3:c.338-212del	NP_149353.1:n.338-212del
NM_033164.3:c.305-212del	NP_149354.1:n.305-212del
NM_033165.3:c.218-212del	NP_149355.1:n.218-212del
XM_011539509.1:c.260-212del	XP_011537811.1:n.260-212del
XR_946252.2:n.585del
XR_946253.2:n.583del
NM_006119.5:c.251-212del	NP_006110.1:n.251-212del
NM_033163.4:c.338-212del	NP_149353.1:n.338-212del
NM_033164.4:c.305-212del	NP_149354.1:n.305-212del
NM_033165.4:c.218-212del	NP_149355.1:n.218-212del
NM_001206389.2:c.26-212del	NP_001193318.1:n.26-212del
NM_006119.6:c.251-212del	NP_006110.1:n.251-212del
NM_033163.5:c.338-212del MANE Select	NP_149353.1:n.338-212del
NM_033165.5:c.218-212del	NP_149355.1:n.218-212del