Canonical Allele Identifier: CA406174835

Gene: ETHE1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43507948C>G , CM000681.2:g.43507948C>G	GRCh38
NC_000019.9:g.44012100C>G , CM000681.1:g.44012100C>G	GRCh37
NC_000019.8:g.48703940C>G	NCBI36
NG_008141.1:g.24297G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292147.7:c.708G>C MANE Select	ENSP00000292147.1:p.Gln236His
ENST00000292147.6:c.708G>C	ENSP00000292147.1:p.Gln236His
ENST00000594342.5:c.*271G>C	ENSP00000469652.1:n.*271G>C
ENST00000598330.1:c.*271G>C	ENSP00000469219.1:n.*271G>C
ENST00000600651.5:c.708G>C	ENSP00000469037.1:p.Gln236His
NM_014297.3:c.708G>C	NP_055112.2:p.Gln236His
XM_005258687.2:c.627G>C	XP_005258744.1:p.Gln209His
XM_005258688.2:c.339G>C	XP_005258745.1:p.Gln113His
XM_011526685.1:c.429G>C	XP_011524987.1:p.Gln143His
NM_001320867.1:c.675G>C	NP_001307796.1:p.Gln225His
NM_001320868.1:c.339G>C	NP_001307797.1:p.Gln113His
NM_001320869.1:c.414G>C	NP_001307798.1:p.Gln138His
NM_014297.4:c.708G>C	NP_055112.2:p.Gln236His
XM_005258687.4:c.627G>C	XP_005258744.1:p.Gln209His
NM_014297.5:c.708G>C MANE Select	NP_055112.2:p.Gln236His
NM_001320867.2:c.675G>C	NP_001307796.1:p.Gln225His
NM_001320868.2:c.339G>C	NP_001307797.1:p.Gln113His
NM_001320869.2:c.414G>C	NP_001307798.1:p.Gln138His