Canonical Allele Identifier: CA406178837

Gene: ETHE1 ZNF575

Linked Data

• MyVariant Identifiers: chr19:g.44030363A>G (hg19) ; chr19:g.43526211A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43526211A>G , CM000681.2:g.43526211A>G	GRCh38
NC_000019.9:g.44030363A>G , CM000681.1:g.44030363A>G	GRCh37
NC_000019.8:g.48722203A>G	NCBI36
NG_008141.1:g.6034T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292147.7:c.365T>C (ETHE1) MANE Select	ENSP00000292147.1:p.Phe122Ser
ENST00000292147.6:c.365T>C (ETHE1)	ENSP00000292147.1:p.Phe122Ser
ENST00000458714.2:c.-93A>G (ZNF575)	ENSP00000413956.2:n.-93A>G
ENST00000594342.5:c.226+304T>C (ETHE1)	ENSP00000469652.1:n.226+304T>C
ENST00000595115.1:n.583T>C (ETHE1)
ENST00000598330.1:c.226+304T>C (ETHE1)	ENSP00000469219.1:n.226+304T>C
ENST00000600651.5:c.365T>C (ETHE1)	ENSP00000469037.1:p.Phe122Ser
ENST00000602138.1:c.*369T>C (ETHE1)	ENSP00000468964.1:n.*369T>C
NM_014297.3:c.365T>C (ETHE1)	NP_055112.2:p.Phe122Ser
XM_005258687.2:c.284T>C (ETHE1)	XP_005258744.1:p.Phe95Ser
XM_005258688.2:c.6+304T>C (ETHE1)	XP_005258745.1:n.6+304T>C
XM_011526685.1:c.226+304T>C (ETHE1)	XP_011524987.1:n.226+304T>C
NM_001320867.1:c.332T>C (ETHE1)	NP_001307796.1:p.Phe111Ser
NM_001320868.1:c.6+304T>C (ETHE1)	NP_001307797.1:n.6+304T>C
NM_001320869.1:c.81+886T>C (ETHE1)	NP_001307798.1:n.81+886T>C
NM_014297.4:c.365T>C (ETHE1)	NP_055112.2:p.Phe122Ser
XM_005258687.4:c.284T>C (ETHE1)	XP_005258744.1:p.Phe95Ser
NM_014297.5:c.365T>C (ETHE1) MANE Select	NP_055112.2:p.Phe122Ser
NM_001320867.2:c.332T>C (ETHE1)	NP_001307796.1:p.Phe111Ser
NM_001320868.2:c.6+304T>C (ETHE1)	NP_001307797.1:n.6+304T>C
NM_001320869.2:c.81+886T>C (ETHE1)	NP_001307798.1:n.81+886T>C