Canonical Allele Identifier: CA507737754

Gene: ETHE1 ZNF575

Linked Data

• MyVariant Identifiers: chr19:g.44030449G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43526297G>A , CM000681.2:g.43526297G>A	GRCh38
NC_000019.9:g.44030449G>A , CM000681.1:g.44030449G>A	GRCh37
NC_000019.8:g.48722289G>A	NCBI36
NG_008141.1:g.5948C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292147.7:c.279C>T (ETHE1) MANE Select	ENSP00000292147.1:p.Ser93=
ENST00000292147.6:c.279C>T (ETHE1)	ENSP00000292147.1:p.Ser93=
ENST00000458714.2:c.-66+59G>A (ZNF575)	ENSP00000413956.2:n.-66+59G>A
ENST00000594342.5:c.226+218C>T (ETHE1)	ENSP00000469652.1:n.226+218C>T
ENST00000595115.1:n.497C>T (ETHE1)
ENST00000598330.1:c.226+218C>T (ETHE1)	ENSP00000469219.1:n.226+218C>T
ENST00000600651.5:c.279C>T (ETHE1)	ENSP00000469037.1:p.Ser93=
ENST00000602138.1:c.*283C>T (ETHE1)	ENSP00000468964.1:n.*283C>T
NM_014297.3:c.279C>T (ETHE1)	NP_055112.2:p.Ser93=
XM_005258687.2:c.198C>T (ETHE1)	XP_005258744.1:p.Ser66=
XM_005258688.2:c.6+218C>T (ETHE1)	XP_005258745.1:n.6+218C>T
XM_011526685.1:c.226+218C>T (ETHE1)	XP_011524987.1:n.226+218C>T
NM_001320867.1:c.246C>T (ETHE1)	NP_001307796.1:p.Ser82=
NM_001320868.1:c.6+218C>T (ETHE1)	NP_001307797.1:n.6+218C>T
NM_001320869.1:c.81+800C>T (ETHE1)	NP_001307798.1:n.81+800C>T
NM_014297.4:c.279C>T (ETHE1)	NP_055112.2:p.Ser93=
XM_005258687.4:c.198C>T (ETHE1)	XP_005258744.1:p.Ser66=
NM_014297.5:c.279C>T (ETHE1) MANE Select	NP_055112.2:p.Ser93=
NM_001320867.2:c.246C>T (ETHE1)	NP_001307796.1:p.Ser82=
NM_001320868.2:c.6+218C>T (ETHE1)	NP_001307797.1:n.6+218C>T
NM_001320869.2:c.81+800C>T (ETHE1)	NP_001307798.1:n.81+800C>T