Canonical Allele Identifier: CA413449449

Gene: EDA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70035391T>C , CM000685.2:g.70035391T>C	GRCh38
NC_000023.10:g.69255241T>C , CM000685.1:g.69255241T>C	GRCh37
NC_000023.9:g.69171966T>C	NCBI36
NG_009809.1:g.424331T>C
NG_009809.2:g.424325T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001399.5:c.958T>C MANE Select	NP_001390.1:p.Tyr320His
ENST00000374552.9:c.958T>C MANE Select	ENSP00000363680.4:p.Tyr320His
NM_001005609.1:c.952T>C	NP_001005609.1:p.Tyr318His
NM_001005609.2:c.952T>C	NP_001005609.1:p.Tyr318His
NM_001005612.2:c.943T>C	NP_001005612.2:p.Tyr315His
NM_001005612.3:c.943T>C	NP_001005612.2:p.Tyr315His
NM_001399.4:c.958T>C	NP_001390.1:p.Tyr320His
ENST00000374552.8:c.958T>C	ENSP00000363680.4:p.Tyr320His
ENST00000374553.6:c.952T>C	ENSP00000363681.2:p.Tyr318His
ENST00000524573.5:c.943T>C	ENSP00000432585.1:p.Tyr315His
ENST00000616899.1:c.562T>C	ENSP00000481963.1:p.Tyr188His
XM_006724630.2:c.949T>C	XP_006724693.1:p.Tyr317His
XM_017029336.1:c.916T>C	XP_016884825.1:p.Tyr306His