Canonical Allele Identifier: CA491323235

Gene: ETFA

Linked Data

• gnomAD v4: 15-76274365-C-G
• MyVariant Identifiers: chr15:g.76566706C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.76274365C>G , CM000677.2:g.76274365C>G	GRCh38
NC_000015.9:g.76566706C>G , CM000677.1:g.76566706C>G	GRCh37
NC_000015.8:g.74353761C>G	NCBI36
NG_007077.2:g.42105G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000559386.2:c.816+47G>C	ENSP00000452777.2:n.816+47G>C
ENST00000560044.6:c.*811+47G>C	ENSP00000452942.1:n.*811+47G>C
ENST00000560595.6:c.1035+47G>C	ENSP00000453345.2:n.1035+47G>C
ENST00000565910.6:c.816+47G>C	ENSP00000458001.2:n.816+47G>C
ENST00000685118.1:c.*811+47G>C	ENSP00000509473.1:n.*811+47G>C
ENST00000685548.1:c.816+47G>C	ENSP00000510343.1:n.816+47G>C
ENST00000685863.1:c.600+47G>C	ENSP00000509361.1:n.600+47G>C
ENST00000687293.1:c.891+47G>C	ENSP00000509928.1:n.891+47G>C
ENST00000687975.1:c.*692+47G>C	ENSP00000508690.1:n.*692+47G>C
ENST00000688154.1:c.816+47G>C	ENSP00000510637.1:n.816+47G>C
ENST00000688389.1:c.747+47G>C	ENSP00000510491.1:n.747+47G>C
ENST00000688637.1:n.897+47G>C
ENST00000688908.1:c.651+47G>C	ENSP00000510242.1:n.651+47G>C
ENST00000689730.1:c.798+47G>C	ENSP00000510006.1:n.798+47G>C
ENST00000689739.1:n.828+47G>C
ENST00000690610.1:c.816+47G>C	ENSP00000510473.1:n.816+47G>C
ENST00000691021.1:c.*811+47G>C	ENSP00000510805.1:n.*811+47G>C
ENST00000691071.1:n.595+47G>C
ENST00000691695.1:c.669+47G>C	ENSP00000509402.1:n.669+47G>C
ENST00000692691.1:c.939+47G>C	ENSP00000508808.1:n.939+47G>C
ENST00000693064.1:c.*791+47G>C	ENSP00000510720.1:n.*791+47G>C
ENST00000557943.6:c.816+47G>C MANE Select	ENSP00000452762.1:n.816+47G>C
ENST00000267950.12:c.*539+47G>C	ENSP00000267950.8:n.*539+47G>C
ENST00000433983.6:c.669+47G>C	ENSP00000399273.2:n.669+47G>C
ENST00000557943.5:c.816+47G>C	ENSP00000452762.1:n.816+47G>C
ENST00000558803.1:n.215G>C
ENST00000559075.5:n.840+47G>C
ENST00000559602.5:c.504+47G>C	ENSP00000452659.1:n.504+47G>C
ENST00000559758.5:n.704G>C
ENST00000559973.5:c.526+47G>C
ENST00000560044.5:c.*811+47G>C	ENSP00000452942.1:n.*811+47G>C
ENST00000560595.5:c.747+47G>C	ENSP00000453345.1:n.747+47G>C
ENST00000560726.5:c.36+47G>C	ENSP00000453098.1:n.36+47G>C
ENST00000560816.5:n.375+47G>C
ENST00000560899.5:c.36+47G>C	ENSP00000453422.1:n.36+47G>C
NM_000126.3:c.816+47G>C	NP_000117.1:n.816+47G>C
NM_001127716.1:c.669+47G>C	NP_001121188.1:n.669+47G>C
XR_931766.1:n.871+47G>C
XR_931766.3:n.897+47G>C
NM_000126.4:c.816+47G>C MANE Select	NP_000117.1:n.816+47G>C
NM_001127716.2:c.669+47G>C	NP_001121188.1:n.669+47G>C