Canonical Allele Identifier: CA406178740

Gene: ETHE1 ZNF575

Linked Data

• ClinVar Variation Id: 2675150
• ClinVar RCV Id: RCV003467951
• MyVariant Identifiers: chr19:g.44030352C>A (hg19) ; chr19:g.43526200C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43526200C>A , CM000681.2:g.43526200C>A	GRCh38
NC_000019.9:g.44030352C>A , CM000681.1:g.44030352C>A	GRCh37
NC_000019.8:g.48722192C>A	NCBI36
NG_008141.1:g.6045G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292147.7:c.375+1G>T (ETHE1) MANE Select	ENSP00000292147.1:n.375+1G>T
ENST00000292147.6:c.375+1G>T (ETHE1)	ENSP00000292147.1:n.375+1G>T
ENST00000458714.2:c.-104C>A (ZNF575)	ENSP00000413956.2:n.-104C>A
ENST00000594342.5:c.226+315G>T (ETHE1)	ENSP00000469652.1:n.226+315G>T
ENST00000598330.1:c.226+315G>T (ETHE1)	ENSP00000469219.1:n.226+315G>T
ENST00000600651.5:c.375+1G>T (ETHE1)	ENSP00000469037.1:n.375+1G>T
ENST00000602138.1:c.*379+1G>T (ETHE1)	ENSP00000468964.1:n.*379+1G>T
NM_014297.3:c.375+1G>T (ETHE1)	NP_055112.2:n.375+1G>T
XM_005258687.2:c.294+1G>T (ETHE1)	XP_005258744.1:n.294+1G>T
XM_005258688.2:c.6+315G>T (ETHE1)	XP_005258745.1:n.6+315G>T
XM_011526685.1:c.226+315G>T (ETHE1)	XP_011524987.1:n.226+315G>T
NM_001320867.1:c.342+1G>T (ETHE1)	NP_001307796.1:n.342+1G>T
NM_001320868.1:c.6+315G>T (ETHE1)	NP_001307797.1:n.6+315G>T
NM_001320869.1:c.81+897G>T (ETHE1)	NP_001307798.1:n.81+897G>T
NM_014297.4:c.375+1G>T (ETHE1)	NP_055112.2:n.375+1G>T
XM_005258687.4:c.294+1G>T (ETHE1)	XP_005258744.1:n.294+1G>T
NM_014297.5:c.375+1G>T (ETHE1) MANE Select	NP_055112.2:n.375+1G>T
NM_001320867.2:c.342+1G>T (ETHE1)	NP_001307796.1:n.342+1G>T
NM_001320868.2:c.6+315G>T (ETHE1)	NP_001307797.1:n.6+315G>T
NM_001320869.2:c.81+897G>T (ETHE1)	NP_001307798.1:n.81+897G>T