Canonical Allele Identifier: CA413450342

Gene: EDA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70035549C>G , CM000685.2:g.70035549C>G	GRCh38
NC_000023.10:g.69255399C>G , CM000685.1:g.69255399C>G	GRCh37
NC_000023.9:g.69172124C>G	NCBI36
NG_009809.1:g.424489C>G
NG_009809.2:g.424483C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001399.5:c.1116C>G MANE Select	NP_001390.1:p.Asn372Lys
ENST00000374552.9:c.1116C>G MANE Select	ENSP00000363680.4:p.Asn372Lys
NM_001005609.1:c.1110C>G	NP_001005609.1:p.Asn370Lys
NM_001005609.2:c.1110C>G	NP_001005609.1:p.Asn370Lys
NM_001005612.2:c.1101C>G	NP_001005612.2:p.Asn367Lys
NM_001005612.3:c.1101C>G	NP_001005612.2:p.Asn367Lys
NM_001399.4:c.1116C>G	NP_001390.1:p.Asn372Lys
ENST00000374552.8:c.1116C>G	ENSP00000363680.4:p.Asn372Lys
ENST00000374553.6:c.1110C>G	ENSP00000363681.2:p.Asn370Lys
ENST00000524573.5:c.1101C>G	ENSP00000432585.1:p.Asn367Lys
ENST00000616899.1:c.720C>G	ENSP00000481963.1:p.Asn240Lys
XM_006724630.2:c.1107C>G	XP_006724693.1:p.Asn369Lys
XM_017029336.1:c.1074C>G	XP_016884825.1:p.Asn358Lys