Canonical Allele Identifier: CA1075634221

Gene: FGF10

Linked Data

• gnomAD v3: 5-44365367-G-T
• gnomAD v4: 5-44365367-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44365367G>T , CM000667.2:g.44365367G>T	GRCh38
NC_000005.9:g.44365469G>T , CM000667.1:g.44365469G>T	GRCh37
NC_000005.8:g.44401226G>T	NCBI36
NG_011446.1:g.28316C>A

Transcript Alleles

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