Canonical Allele Identifier: CA9487828

Gene: ETHE1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43508835G>A , CM000681.2:g.43508835G>A	GRCh38
NC_000019.9:g.44012987G>A , CM000681.1:g.44012987G>A	GRCh37
NC_000019.8:g.48704827G>A	NCBI36
NG_008141.1:g.23410C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_014297.5:c.535C>T MANE Select	NP_055112.2:p.His179Tyr
ENST00000292147.7:c.535C>T MANE Select	ENSP00000292147.1:p.His179Tyr
NM_001320867.1:c.502C>T	NP_001307796.1:p.His168Tyr
NM_001320867.2:c.502C>T	NP_001307796.1:p.His168Tyr
NM_001320868.1:c.166C>T	NP_001307797.1:p.His56Tyr
NM_001320868.2:c.166C>T	NP_001307797.1:p.His56Tyr
NM_001320869.1:c.241C>T	NP_001307798.1:p.His81Tyr
NM_001320869.2:c.241C>T	NP_001307798.1:p.His81Tyr
NM_014297.3:c.535C>T	NP_055112.2:p.His179Tyr
NM_014297.4:c.535C>T	NP_055112.2:p.His179Tyr
ENST00000292147.6:c.535C>T	ENSP00000292147.1:p.His179Tyr
ENST00000594342.5:c.*98C>T	ENSP00000469652.1:n.*98C>T
ENST00000598330.1:c.*98C>T	ENSP00000469219.1:n.*98C>T
ENST00000600651.5:c.535C>T	ENSP00000469037.1:p.His179Tyr
XM_005258687.2:c.454C>T	XP_005258744.1:p.His152Tyr
XM_005258687.4:c.454C>T	XP_005258744.1:p.His152Tyr
XM_005258688.2:c.166C>T	XP_005258745.1:p.His56Tyr
XM_011526685.1:c.256C>T	XP_011524987.1:p.His86Tyr