Canonical Allele Identifier: CA2337530579

Gene: ETHE1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43508067G= , CM000681.2:g.43508067G=	GRCh38
NC_000019.9:g.44012219G= , CM000681.1:g.44012219G=	GRCh37
NC_000019.8:g.48704059G=	NCBI36
NG_008141.1:g.24178C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000292147.7:c.596-7C= MANE Select	ENSP00000292147.1:n.596-7C=
ENST00000292147.6:c.596-7C=	ENSP00000292147.1:n.596-7C=
ENST00000594342.5:c.*159-7C=	ENSP00000469652.1:n.*159-7C=
ENST00000598330.1:c.*159-7C=	ENSP00000469219.1:n.*159-7C=
ENST00000600651.5:c.596-7C=	ENSP00000469037.1:n.596-7C=
NM_014297.3:c.596-7C=	NP_055112.2:n.596-7C=
XM_005258687.2:c.515-7C=	XP_005258744.1:n.515-7C=
XM_005258688.2:c.227-7C=	XP_005258745.1:n.227-7C=
XM_011526685.1:c.317-7C=	XP_011524987.1:n.317-7C=
NM_001320867.1:c.563-7C=	NP_001307796.1:n.563-7C=
NM_001320868.1:c.227-7C=	NP_001307797.1:n.227-7C=
NM_001320869.1:c.302-7C=	NP_001307798.1:n.302-7C=
NM_014297.4:c.596-7C=	NP_055112.2:n.596-7C=
XM_005258687.4:c.515-7C=	XP_005258744.1:n.515-7C=
NM_014297.5:c.596-7C= MANE Select	NP_055112.2:n.596-7C=
NM_001320867.2:c.563-7C=	NP_001307796.1:n.563-7C=
NM_001320868.2:c.227-7C=	NP_001307797.1:n.227-7C=
NM_001320869.2:c.302-7C=	NP_001307798.1:n.302-7C=