Canonical Allele Identifier: CA633265055
Gene: ETHE1 HGNC NCBI
ZNF575 HGNC NCBI

Linked Data

dbSNP Id: rs1217619510

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.43526051dup , CM000681.2:g.43526051dup GRCh38
NC_000019.9:g.44030203dup , CM000681.1:g.44030203dup GRCh37
NC_000019.8:g.48722043dup NCBI36
NG_008141.1:g.6199dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000292147.7:c.375+155dup (ETHE1) MANE Select ENSP00000292147.1:n.375+155dup
ENST00000292147.6:c.375+155dup (ETHE1) ENSP00000292147.1:n.375+155dup
ENST00000458714.2:c.-253dup (ZNF575) ENSP00000413956.2:n.-253dup
ENST00000594342.5:c.226+469dup (ETHE1) ENSP00000469652.1:n.226+469dup
ENST00000598330.1:c.226+469dup (ETHE1) ENSP00000469219.1:n.226+469dup
ENST00000600651.5:c.375+155dup (ETHE1) ENSP00000469037.1:n.375+155dup
ENST00000602138.1:c.*379+155dup (ETHE1) ENSP00000468964.1:n.*379+155dup
NM_014297.3:c.375+155dup (ETHE1) NP_055112.2:n.375+155dup
XM_005258687.2:c.294+155dup (ETHE1) XP_005258744.1:n.294+155dup
XM_005258688.2:c.6+469dup (ETHE1) XP_005258745.1:n.6+469dup
XM_011526685.1:c.226+469dup (ETHE1) XP_011524987.1:n.226+469dup
NM_001320867.1:c.342+155dup (ETHE1) NP_001307796.1:n.342+155dup
NM_001320868.1:c.6+469dup (ETHE1) NP_001307797.1:n.6+469dup
NM_001320869.1:c.81+1051dup (ETHE1) NP_001307798.1:n.81+1051dup
NM_014297.4:c.375+155dup (ETHE1) NP_055112.2:n.375+155dup
XM_005258687.4:c.294+155dup (ETHE1) XP_005258744.1:n.294+155dup
NM_014297.5:c.375+155dup (ETHE1) MANE Select NP_055112.2:n.375+155dup
NM_001320867.2:c.342+155dup (ETHE1) NP_001307796.1:n.342+155dup
NM_001320868.2:c.6+469dup (ETHE1) NP_001307797.1:n.6+469dup
NM_001320869.2:c.81+1051dup (ETHE1) NP_001307798.1:n.81+1051dup