Canonical Allele Identifier: CA1075634213
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs1741583384

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44365367_44365375del , CM000667.2:g.44365367_44365375del GRCh38
NC_000005.9:g.44365469_44365477del , CM000667.1:g.44365469_44365477del GRCh37
NC_000005.8:g.44401226_44401234del NCBI36
NG_011446.1:g.28308_28316del

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.325+22983_325+22991del MANE Select ENSP00000264664.4:n.325+22983_325+22991del
ENST00000264664.4:c.325+22983_325+22991del ENSP00000264664.4:n.325+22983_325+22991del
NM_004465.1:c.325+22983_325+22991del NP_004456.1:n.325+22983_325+22991del
XM_005248264.2:c.325+22983_325+22991del XP_005248321.1:n.325+22983_325+22991del
XM_005248264.4:c.325+22983_325+22991del XP_005248321.1:n.325+22983_325+22991del
NM_004465.2:c.325+22983_325+22991del MANE Select NP_004456.1:n.325+22983_325+22991del