Canonical Allele Identifier: CA413447897

Gene: EDA

Linked Data

• MyVariant Identifiers: chrX:g.69176913C>T (hg19) ; chrX:g.69957063C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.69957063C>T , CM000685.2:g.69957063C>T	GRCh38
NC_000023.10:g.69176913C>T , CM000685.1:g.69176913C>T	GRCh37
NC_000023.9:g.69093638C>T	NCBI36
NG_009809.1:g.346003C>T
NG_009809.2:g.345997C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374552.9:c.433C>T MANE Select	ENSP00000363680.4:p.Pro145Ser
ENST00000374548.5:n.675C>T
ENST00000374552.8:c.433C>T	ENSP00000363680.4:p.Pro145Ser
ENST00000374553.6:c.433C>T	ENSP00000363681.2:p.Pro145Ser
ENST00000502251.5:n.726C>T
ENST00000503592.5:c.37C>T	ENSP00000423037.1:p.Pro13Ser
ENST00000524573.5:c.433C>T	ENSP00000432585.1:p.Pro145Ser
ENST00000533317.5:n.1048C>T
ENST00000616899.1:c.37C>T	ENSP00000481963.1:p.Pro13Ser
NM_001005609.1:c.433C>T	NP_001005609.1:p.Pro145Ser
NM_001005612.2:c.433C>T	NP_001005612.2:p.Pro145Ser
NM_001399.4:c.433C>T	NP_001390.1:p.Pro145Ser
XM_006724630.2:c.433C>T	XP_006724693.1:p.Pro145Ser
XM_011530885.1:c.433C>T	XP_011529187.1:p.Pro145Ser
XM_011530885.2:c.433C>T	XP_011529187.1:p.Pro145Ser
XM_017029336.1:c.433C>T	XP_016884825.1:p.Pro145Ser
NM_001399.5:c.433C>T MANE Select	NP_001390.1:p.Pro145Ser
NM_001005609.2:c.433C>T	NP_001005609.1:p.Pro145Ser
NM_001005612.3:c.433C>T	NP_001005612.2:p.Pro145Ser