Canonical Allele Identifier: CA2585521749
Gene: ETHE1 HGNC NCBI
ZNF575 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.43527082T>C , CM000681.2:g.43527082T>C GRCh38
NC_000019.9:g.44031234T>C , CM000681.1:g.44031234T>C GRCh37
NC_000019.8:g.48723074T>C NCBI36
NG_008141.1:g.5163A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000292147.7:c.81+15A>G (ETHE1) MANE Select ENSP00000292147.1:n.81+15A>G
ENST00000292147.6:c.81+15A>G (ETHE1) ENSP00000292147.1:n.81+15A>G
ENST00000458714.2:c.135+456T>C (ZNF575) ENSP00000413956.2:n.135+456T>C
ENST00000594342.5:c.81+15A>G (ETHE1) ENSP00000469652.1:n.81+15A>G
ENST00000595115.1:n.134+15A>G (ETHE1)
ENST00000598330.1:c.81+15A>G (ETHE1) ENSP00000469219.1:n.81+15A>G
ENST00000600651.5:c.81+15A>G (ETHE1) ENSP00000469037.1:n.81+15A>G
ENST00000602138.1:c.96A>G (ETHE1) ENSP00000468964.1:p.Gly32=
NM_014297.3:c.81+15A>G (ETHE1) NP_055112.2:n.81+15A>G
XM_005258687.2:c.-146A>G (ETHE1) XP_005258744.1:n.-146A>G
XM_005258688.2:c.-140+15A>G (ETHE1) XP_005258745.1:n.-140+15A>G
XM_011526685.1:c.81+15A>G (ETHE1) XP_011524987.1:n.81+15A>G
NM_001320867.1:c.81+15A>G (ETHE1) NP_001307796.1:n.81+15A>G
NM_001320868.1:c.-140+15A>G (ETHE1) NP_001307797.1:n.-140+15A>G
NM_001320869.1:c.81+15A>G (ETHE1) NP_001307798.1:n.81+15A>G
NM_014297.4:c.81+15A>G (ETHE1) NP_055112.2:n.81+15A>G
XM_005258687.4:c.-146A>G (ETHE1) XP_005258744.1:n.-146A>G
NM_014297.5:c.81+15A>G (ETHE1) MANE Select NP_055112.2:n.81+15A>G
NM_001320867.2:c.81+15A>G (ETHE1) NP_001307796.1:n.81+15A>G
NM_001320868.2:c.-140+15A>G (ETHE1) NP_001307797.1:n.-140+15A>G
NM_001320869.2:c.81+15A>G (ETHE1) NP_001307798.1:n.81+15A>G