Canonical Allele Identifier: CA1106076553

Gene: FOXP2

Linked Data

• gnomAD v3: 7-114100933-A-ACTTC
• gnomAD v4: 7-114100933-A-ACTTC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114100933_114100934insCTTC , CM000669.2:g.114100933_114100934insCTTC	GRCh38
NC_000007.13:g.113740988_113740989insCTTC , CM000669.1:g.113740988_113740989insCTTC	GRCh37
NC_000007.12:g.113528224_113528225insCTTC	NCBI36
NG_007491.2:g.19624_19625insCTTC
NG_007491.3:g.19624_19625insCTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703612.1:c.-247+14322_-247+14323insCTTC	ENSP00000515396.1:n.-247+14322_-247+14323insCTTC
ENST00000703613.1:c.-365+14322_-365+14323insCTTC	ENSP00000515397.1:n.-365+14322_-365+14323insCTTC
ENST00000703614.1:c.-247+14322_-247+14323insCTTC	ENSP00000515398.1:n.-247+14322_-247+14323insCTTC
ENST00000703615.1:c.-365+14322_-365+14323insCTTC	ENSP00000515399.1:n.-365+14322_-365+14323insCTTC
ENST00000703616.1:c.-247+13095_-247+13096insCTTC	ENSP00000515400.1:n.-247+13095_-247+13096insCTTC
ENST00000412402.5:c.-102+14322_-102+14323insCTTC	ENSP00000405470.1:n.-102+14322_-102+14323insCTTC
ENST00000440349.5:c.-247+14322_-247+14323insCTTC	ENSP00000395552.1:n.-247+14322_-247+14323insCTTC
ENST00000441290.6:c.-435+14322_-435+14323insCTTC	ENSP00000416825.1:n.-435+14322_-435+14323insCTTC
ENST00000495516.1:n.105+12663_105+12664insCTTC
ENST00000635638.1:c.-247+13095_-247+13096insCTTC	ENSP00000489073.1:n.-247+13095_-247+13096insCTTC
NR_033766.1:n.302+14322_302+14323insCTTC
XM_011516706.1:c.-360+14322_-360+14323insCTTC	XP_011515008.1:n.-360+14322_-360+14323insCTTC
XM_017012801.2:c.-247+12505_-247+12506insCTTC	XP_016868290.1:n.-247+12505_-247+12506insCTTC
NR_033766.2:n.285+14322_285+14323insCTTC