Canonical Allele Identifier: CA2629673120

Gene: ETFA

Linked Data

• gnomAD v4: 15-76285578-TAAAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.76285586_76285589del , CM000677.2:g.76285586_76285589del	GRCh38
NC_000015.9:g.76577927_76577930del , CM000677.1:g.76577927_76577930del	GRCh37
NC_000015.8:g.74364982_74364985del	NCBI36
NG_007077.2:g.30888_30891del

Transcript Alleles

HGVS	Amino-acid change
ENST00000559386.2:c.664+55_664+58del	ENSP00000452777.2:n.664+55_664+58del
ENST00000560044.6:c.*659+55_*659+58del	ENSP00000452942.1:n.*659+55_*659+58del
ENST00000560595.6:c.664+55_664+58del	ENSP00000453345.2:n.664+55_664+58del
ENST00000565910.6:c.664+55_664+58del	ENSP00000458001.2:n.664+55_664+58del
ENST00000685118.1:c.*659+55_*659+58del	ENSP00000509473.1:n.*659+55_*659+58del
ENST00000685548.1:c.664+55_664+58del	ENSP00000510343.1:n.664+55_664+58del
ENST00000685863.1:c.517+55_517+58del	ENSP00000509361.1:n.517+55_517+58del
ENST00000687293.1:c.664+55_664+58del	ENSP00000509928.1:n.664+55_664+58del
ENST00000687975.1:c.*540+55_*540+58del	ENSP00000508690.1:n.*540+55_*540+58del
ENST00000688154.1:c.664+55_664+58del	ENSP00000510637.1:n.664+55_664+58del
ENST00000688389.1:c.664+55_664+58del	ENSP00000510491.1:n.664+55_664+58del
ENST00000688637.1:n.745+55_745+58del
ENST00000688908.1:c.499+55_499+58del	ENSP00000510242.1:n.499+55_499+58del
ENST00000689120.1:n.748+55_748+58del
ENST00000689730.1:c.646+55_646+58del	ENSP00000510006.1:n.646+55_646+58del
ENST00000689739.1:n.745+55_745+58del
ENST00000690610.1:c.664+55_664+58del	ENSP00000510473.1:n.664+55_664+58del
ENST00000691021.1:c.*659+55_*659+58del	ENSP00000510805.1:n.*659+55_*659+58del
ENST00000691071.1:n.443+55_443+58del
ENST00000691695.1:c.517+55_517+58del	ENSP00000509402.1:n.517+55_517+58del
ENST00000692691.1:c.664+55_664+58del	ENSP00000508808.1:n.664+55_664+58del
ENST00000693064.1:c.*639+55_*639+58del	ENSP00000510720.1:n.*639+55_*639+58del
ENST00000557943.6:c.664+55_664+58del MANE Select	ENSP00000452762.1:n.664+55_664+58del
ENST00000267950.12:c.*387+55_*387+58del	ENSP00000267950.8:n.*387+55_*387+58del
ENST00000433983.6:c.517+55_517+58del	ENSP00000399273.2:n.517+55_517+58del
ENST00000557943.5:c.664+55_664+58del	ENSP00000452762.1:n.664+55_664+58del
ENST00000559075.5:n.688+55_688+58del
ENST00000559386.1:c.664+55_664+58del	ENSP00000452777.1:n.664+55_664+58del
ENST00000559602.5:c.352+55_352+58del	ENSP00000452659.1:n.352+55_352+58del
ENST00000559758.5:n.505+55_505+58del
ENST00000559973.5:c.374+55_374+58del
ENST00000560044.5:c.*659+55_*659+58del	ENSP00000452942.1:n.*659+55_*659+58del
ENST00000560345.5:c.476+55_476+58del
ENST00000560595.5:c.664+55_664+58del	ENSP00000453345.1:n.664+55_664+58del
ENST00000560726.5:c.-117+55_-117+58del	ENSP00000453098.1:n.-117+55_-117+58del
ENST00000560816.5:n.223+55_223+58del
ENST00000560899.5:c.-117+55_-117+58del	ENSP00000453422.1:n.-117+55_-117+58del
NM_000126.3:c.664+55_664+58del	NP_000117.1:n.664+55_664+58del
NM_001127716.1:c.517+55_517+58del	NP_001121188.1:n.517+55_517+58del
XR_931766.1:n.719+55_719+58del
XR_931766.3:n.745+55_745+58del
NM_000126.4:c.664+55_664+58del MANE Select	NP_000117.1:n.664+55_664+58del
NM_001127716.2:c.517+55_517+58del	NP_001121188.1:n.517+55_517+58del