Canonical Allele Identifier: CA658653770

Gene: EVC

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5741782_5741785delinsTTAC , CM000666.2:g.5741782_5741785delinsTTAC	GRCh38
NC_000004.11:g.5743509_5743512delinsTTAC , CM000666.1:g.5743509_5743512delinsTTAC	GRCh37
NC_000004.10:g.5794410_5794413delinsTTAC	NCBI36
NG_008843.1:g.35586_35589delinsTTAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264956.11:c.769_772delinsTTAC MANE Select	ENSP00000264956.6:p.Tyr258His
ENST00000264956.10:c.769_772delinsTTAC	ENSP00000264956.6:p.Tyr258His
ENST00000509451.1:c.769_772delinsTTAC	ENSP00000426774.1:p.Tyr258His
NM_001306090.1:c.769_772delinsTTAC	NP_001293019.1:p.Tyr258His
NM_001306092.1:c.769_772delinsTTAC	NP_001293021.1:p.Tyr258His
NM_153717.2:c.769_772delinsTTAC	NP_714928.1:p.Tyr258His
XM_006713865.2:c.769_772delinsTTAC	XP_006713928.1:p.Tyr258His
XM_006713866.2:c.769_772delinsTTAC	XP_006713929.1:p.Tyr258His
XM_011513419.1:c.769_772delinsTTAC	XP_011511721.1:p.Tyr258His
XR_427473.2:n.959_962delinsTTAC
XR_427475.2:n.959_962delinsTTAC
XR_427476.2:n.959_962delinsTTAC
XR_924920.1:n.959_962delinsTTAC
XR_924921.1:n.959_962delinsTTAC
XR_924922.1:n.959_962delinsTTAC
XR_924923.1:n.959_962delinsTTAC
XR_924924.1:n.959_962delinsTTAC
XR_924925.1:n.959_962delinsTTAC
XR_924926.1:n.959_962delinsTTAC
XR_924927.1:n.959_962delinsTTAC
XR_924928.1:n.961_964delinsTTAC
XM_006713865.3:c.769_772delinsTTAC	XP_006713928.1:p.Tyr258His
XM_006713866.3:c.769_772delinsTTAC	XP_006713929.1:p.Tyr258His
XM_011513419.2:c.769_772delinsTTAC	XP_011511721.1:p.Tyr258His
XM_017007883.2:c.769_772delinsTTAC	XP_016863372.1:p.Tyr258His
XR_001741164.1:n.949_952delinsTTAC
XR_001741165.1:n.949_952delinsTTAC
XR_001741166.1:n.949_952delinsTTAC
XR_001741167.1:n.949_952delinsTTAC
XR_001741168.1:n.949_952delinsTTAC
XR_001741169.2:n.951_954delinsTTAC
XR_001741170.1:n.951_954delinsTTAC
XR_427473.3:n.949_952delinsTTAC
XR_427475.3:n.949_952delinsTTAC
XR_427476.3:n.949_952delinsTTAC
XR_924920.2:n.949_952delinsTTAC
XR_924921.2:n.949_952delinsTTAC
XR_924922.2:n.949_952delinsTTAC
XR_924924.2:n.949_952delinsTTAC
XR_924925.2:n.949_952delinsTTAC
XR_924926.2:n.949_952delinsTTAC
NM_153717.3:c.769_772delinsTTAC MANE Select	NP_714928.1:p.Tyr258His
NM_001306090.2:c.769_772delinsTTAC	NP_001293019.1:p.Tyr258His
NM_001306092.2:c.769_772delinsTTAC	NP_001293021.1:p.Tyr258His