Canonical Allele Identifier: CA558944830

Gene: FGF10

Linked Data

• gnomAD v2: 5-44365466-AAAGAGAGAGGT-A
• gnomAD v3: 5-44365364-AAAGAGAGAGGT-A
• gnomAD v4: 5-44365364-AAAGAGAGAGGT-A
• MyVariant Identifiers: chr5:g.44365467_44365477del (hg19) ; chr5:g.44365365_44365375del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44365367_44365377del , CM000667.2:g.44365367_44365377del	GRCh38
NC_000005.9:g.44365469_44365479del , CM000667.1:g.44365469_44365479del	GRCh37
NC_000005.8:g.44401226_44401236del	NCBI36
NG_011446.1:g.28308_28318del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264664.5:c.325+22983_325+22993del MANE Select	ENSP00000264664.4:n.325+22983_325+22993del
ENST00000264664.4:c.325+22983_325+22993del	ENSP00000264664.4:n.325+22983_325+22993del
NM_004465.1:c.325+22983_325+22993del	NP_004456.1:n.325+22983_325+22993del
XM_005248264.2:c.325+22983_325+22993del	XP_005248321.1:n.325+22983_325+22993del
XM_005248264.4:c.325+22983_325+22993del	XP_005248321.1:n.325+22983_325+22993del
NM_004465.2:c.325+22983_325+22993del MANE Select	NP_004456.1:n.325+22983_325+22993del