Canonical Allele Identifier: CA2337530572

Gene: ETHE1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43508056G= , CM000681.2:g.43508056G=	GRCh38
NC_000019.9:g.44012208G= , CM000681.1:g.44012208G=	GRCh37
NC_000019.8:g.48704048G=	NCBI36
NG_008141.1:g.24189C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292147.7:c.600C= MANE Select	ENSP00000292147.1:p.Phe200=
ENST00000292147.6:c.600C=	ENSP00000292147.1:p.Phe200=
ENST00000594342.5:c.*163C=	ENSP00000469652.1:n.*163C=
ENST00000598330.1:c.*163C=	ENSP00000469219.1:n.*163C=
ENST00000600651.5:c.600C=	ENSP00000469037.1:p.Phe200=
NM_014297.3:c.600C=	NP_055112.2:p.Phe200=
XM_005258687.2:c.519C=	XP_005258744.1:p.Phe173=
XM_005258688.2:c.231C=	XP_005258745.1:p.Phe77=
XM_011526685.1:c.321C=	XP_011524987.1:p.Phe107=
NM_001320867.1:c.567C=	NP_001307796.1:p.Phe189=
NM_001320868.1:c.231C=	NP_001307797.1:p.Phe77=
NM_001320869.1:c.306C=	NP_001307798.1:p.Phe102=
NM_014297.4:c.600C=	NP_055112.2:p.Phe200=
XM_005258687.4:c.519C=	XP_005258744.1:p.Phe173=
NM_014297.5:c.600C= MANE Select	NP_055112.2:p.Phe200=
NM_001320867.2:c.567C=	NP_001307796.1:p.Phe189=
NM_001320868.2:c.231C=	NP_001307797.1:p.Phe77=
NM_001320869.2:c.306C=	NP_001307798.1:p.Phe102=