Canonical Allele Identifier: CA1543128949
Gene: FGF10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44365368_44365375delinsAGAGAGGT , CM000667.2:g.44365368_44365375delinsAGAGAGGT GRCh38
NC_000005.9:g.44365470_44365477delinsAGAGAGGT , CM000667.1:g.44365470_44365477delinsAGAGAGGT GRCh37
NC_000005.8:g.44401227_44401234delinsAGAGAGGT NCBI36
NG_011446.1:g.28308_28315delinsACCTCTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.325+22983_325+22990delinsACCTCTCT MANE Select ENSP00000264664.4:n.325+22983_325+22990delinsACCTCTCT
ENST00000264664.4:c.325+22983_325+22990delinsACCTCTCT ENSP00000264664.4:n.325+22983_325+22990delinsACCTCTCT
NM_004465.1:c.325+22983_325+22990delinsACCTCTCT NP_004456.1:n.325+22983_325+22990delinsACCTCTCT
XM_005248264.2:c.325+22983_325+22990delinsACCTCTCT XP_005248321.1:n.325+22983_325+22990delinsACCTCTCT
XM_005248264.4:c.325+22983_325+22990delinsACCTCTCT XP_005248321.1:n.325+22983_325+22990delinsACCTCTCT
NM_004465.2:c.325+22983_325+22990delinsACCTCTCT MANE Select NP_004456.1:n.325+22983_325+22990delinsACCTCTCT
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