Canonical Allele Identifier: CA1435469733

Gene: EVC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5711757_5711763delinsGGTGCCT , CM000666.2:g.5711757_5711763delinsGGTGCCT	GRCh38
NC_000004.11:g.5713484_5713490delinsGGTGCCT , CM000666.1:g.5713484_5713490delinsGGTGCCT	GRCh37
NC_000004.10:g.5764385_5764391delinsGGTGCCT	NCBI36
NG_008843.1:g.5561_5567delinsGGTGCCT
NG_015821.1:g.2786_2792delinsAGGCACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264956.11:c.174+203_174+209delinsGGTGCCT MANE Select	ENSP00000264956.6:n.174+203_174+209delinsGGTGCCT
ENST00000264956.10:c.174+203_174+209delinsGGTGCCT	ENSP00000264956.6:n.174+203_174+209delinsGGTGCCT
ENST00000509451.1:c.174+203_174+209delinsGGTGCCT	ENSP00000426774.1:n.174+203_174+209delinsGGTGCCT
NM_001306090.1:c.174+203_174+209delinsGGTGCCT	NP_001293019.1:n.174+203_174+209delinsGGTGCCT
NM_001306092.1:c.174+203_174+209delinsGGTGCCT	NP_001293021.1:n.174+203_174+209delinsGGTGCCT
NM_153717.2:c.174+203_174+209delinsGGTGCCT	NP_714928.1:n.174+203_174+209delinsGGTGCCT
XM_006713865.2:c.174+203_174+209delinsGGTGCCT	XP_006713928.1:n.174+203_174+209delinsGGTGCCT
XM_006713866.2:c.174+203_174+209delinsGGTGCCT	XP_006713929.1:n.174+203_174+209delinsGGTGCCT
XM_011513419.1:c.174+203_174+209delinsGGTGCCT	XP_011511721.1:n.174+203_174+209delinsGGTGCCT
XR_427473.2:n.364+203_364+209delinsGGTGCCT
XR_427475.2:n.364+203_364+209delinsGGTGCCT
XR_427476.2:n.364+203_364+209delinsGGTGCCT
XR_924920.1:n.364+203_364+209delinsGGTGCCT
XR_924921.1:n.364+203_364+209delinsGGTGCCT
XR_924922.1:n.364+203_364+209delinsGGTGCCT
XR_924923.1:n.364+203_364+209delinsGGTGCCT
XR_924924.1:n.364+203_364+209delinsGGTGCCT
XR_924925.1:n.364+203_364+209delinsGGTGCCT
XR_924926.1:n.364+203_364+209delinsGGTGCCT
XR_924927.1:n.364+203_364+209delinsGGTGCCT
XR_924928.1:n.366+203_366+209delinsGGTGCCT
XM_006713865.3:c.174+203_174+209delinsGGTGCCT	XP_006713928.1:n.174+203_174+209delinsGGTGCCT
XM_006713866.3:c.174+203_174+209delinsGGTGCCT	XP_006713929.1:n.174+203_174+209delinsGGTGCCT
XM_011513419.2:c.174+203_174+209delinsGGTGCCT	XP_011511721.1:n.174+203_174+209delinsGGTGCCT
XM_017007883.2:c.174+203_174+209delinsGGTGCCT	XP_016863372.1:n.174+203_174+209delinsGGTGCCT
XR_001741164.1:n.354+203_354+209delinsGGTGCCT
XR_001741165.1:n.354+203_354+209delinsGGTGCCT
XR_001741166.1:n.354+203_354+209delinsGGTGCCT
XR_001741167.1:n.354+203_354+209delinsGGTGCCT
XR_001741168.1:n.354+203_354+209delinsGGTGCCT
XR_001741169.2:n.356+203_356+209delinsGGTGCCT
XR_001741170.1:n.356+203_356+209delinsGGTGCCT
XR_427473.3:n.354+203_354+209delinsGGTGCCT
XR_427475.3:n.354+203_354+209delinsGGTGCCT
XR_427476.3:n.354+203_354+209delinsGGTGCCT
XR_924920.2:n.354+203_354+209delinsGGTGCCT
XR_924921.2:n.354+203_354+209delinsGGTGCCT
XR_924922.2:n.354+203_354+209delinsGGTGCCT
XR_924924.2:n.354+203_354+209delinsGGTGCCT
XR_924925.2:n.354+203_354+209delinsGGTGCCT
XR_924926.2:n.354+203_354+209delinsGGTGCCT
NM_153717.3:c.174+203_174+209delinsGGTGCCT MANE Select	NP_714928.1:n.174+203_174+209delinsGGTGCCT
NM_001306090.2:c.174+203_174+209delinsGGTGCCT	NP_001293019.1:n.174+203_174+209delinsGGTGCCT
NM_001306092.2:c.174+203_174+209delinsGGTGCCT	NP_001293021.1:n.174+203_174+209delinsGGTGCCT