Canonical Allele Identifier: CA1543128941
Gene: FGF10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44365356A= , CM000667.2:g.44365356A= GRCh38
NC_000005.9:g.44365458A= , CM000667.1:g.44365458A= GRCh37
NC_000005.8:g.44401215A= NCBI36
NG_011446.1:g.28327T=

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.325+23002T= MANE Select ENSP00000264664.4:n.325+23002T=
ENST00000264664.4:c.325+23002T= ENSP00000264664.4:n.325+23002T=
NM_004465.1:c.325+23002T= NP_004456.1:n.325+23002T=
XM_005248264.2:c.325+23002T= XP_005248321.1:n.325+23002T=
XM_005248264.4:c.325+23002T= XP_005248321.1:n.325+23002T=
NM_004465.2:c.325+23002T= MANE Select NP_004456.1:n.325+23002T=
Search 100 bp 5'
Search 100 bp 3'