Canonical Allele Identifier: CA650046662
Gene: FGF10 HGNC NCBI

Linked Data

COSMIC: COSN6511693
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44359421T>C , CM000667.2:g.44359421T>C GRCh38
NC_000005.9:g.44359523T>C , CM000667.1:g.44359523T>C GRCh37
NC_000005.8:g.44395280T>C NCBI36
NG_011446.1:g.34262A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.325+28937A>G MANE Select ENSP00000264664.4:n.325+28937A>G
ENST00000264664.4:c.325+28937A>G ENSP00000264664.4:n.325+28937A>G
NM_004465.1:c.325+28937A>G NP_004456.1:n.325+28937A>G
XM_005248264.2:c.325+28937A>G XP_005248321.1:n.325+28937A>G
XM_005248264.4:c.325+28937A>G XP_005248321.1:n.325+28937A>G
NM_004465.2:c.325+28937A>G MANE Select NP_004456.1:n.325+28937A>G
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