Canonical Allele Identifier: CA811000295
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs386403712
MyVariant Identifiers: chr5:g.44365467_44365468insAAAG (hg19) chr5:g.44365365_44365366insAAAG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44365366_44365367insAAGA , CM000667.2:g.44365366_44365367insAAGA GRCh38
NC_000005.9:g.44365468_44365469insAAGA , CM000667.1:g.44365468_44365469insAAGA GRCh37
NC_000005.8:g.44401225_44401226insAAGA NCBI36
NG_011446.1:g.28317_28318insCTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.325+22992_325+22993insCTTT MANE Select ENSP00000264664.4:n.325+22992_325+22993insCTTT
ENST00000264664.4:c.325+22992_325+22993insCTTT ENSP00000264664.4:n.325+22992_325+22993insCTTT
NM_004465.1:c.325+22992_325+22993insCTTT NP_004456.1:n.325+22992_325+22993insCTTT
XM_005248264.2:c.325+22992_325+22993insCTTT XP_005248321.1:n.325+22992_325+22993insCTTT
XM_005248264.4:c.325+22992_325+22993insCTTT XP_005248321.1:n.325+22992_325+22993insCTTT
NM_004465.2:c.325+22992_325+22993insCTTT MANE Select NP_004456.1:n.325+22992_325+22993insCTTT
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