Canonical Allele Identifier: CA1435469530
Gene: EVC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.5711452_5711467delinsGCCCGCCCTGCTGGCC , CM000666.2:g.5711452_5711467delinsGCCCGCCCTGCTGGCC GRCh38
NC_000004.11:g.5713179_5713194delinsGCCCGCCCTGCTGGCC , CM000666.1:g.5713179_5713194delinsGCCCGCCCTGCTGGCC GRCh37
NC_000004.10:g.5764080_5764095delinsGCCCGCCCTGCTGGCC NCBI36
NG_008843.1:g.5256_5271delinsGCCCGCCCTGCTGGCC
NG_015821.1:g.3082_3097delinsGGCCAGCAGGGCGGGC

Transcript Alleles

HGVS Amino-acid change
ENST00000264956.11:c.72_87delinsGCCCGCCCTGCTGGCC MANE Select ENSP00000264956.6:p.Ala24=
ENST00000264956.10:c.72_87delinsGCCCGCCCTGCTGGCC ENSP00000264956.6:p.Ala24=
ENST00000509451.1:c.72_87delinsGCCCGCCCTGCTGGCC ENSP00000426774.1:p.Ala24=
NM_001306090.1:c.72_87delinsGCCCGCCCTGCTGGCC NP_001293019.1:p.Ala24=
NM_001306092.1:c.72_87delinsGCCCGCCCTGCTGGCC NP_001293021.1:p.Ala24=
NM_153717.2:c.72_87delinsGCCCGCCCTGCTGGCC NP_714928.1:p.Ala24=
XM_006713865.2:c.72_87delinsGCCCGCCCTGCTGGCC XP_006713928.1:p.Ala24=
XM_006713866.2:c.72_87delinsGCCCGCCCTGCTGGCC XP_006713929.1:p.Ala24=
XM_011513419.1:c.72_87delinsGCCCGCCCTGCTGGCC XP_011511721.1:p.Ala24=
XR_427473.2:n.262_277delinsGCCCGCCCTGCTGGCC
XR_427475.2:n.262_277delinsGCCCGCCCTGCTGGCC
XR_427476.2:n.262_277delinsGCCCGCCCTGCTGGCC
XR_924920.1:n.262_277delinsGCCCGCCCTGCTGGCC
XR_924921.1:n.262_277delinsGCCCGCCCTGCTGGCC
XR_924922.1:n.262_277delinsGCCCGCCCTGCTGGCC
XR_924923.1:n.262_277delinsGCCCGCCCTGCTGGCC
XR_924924.1:n.262_277delinsGCCCGCCCTGCTGGCC
XR_924925.1:n.262_277delinsGCCCGCCCTGCTGGCC
XR_924926.1:n.262_277delinsGCCCGCCCTGCTGGCC
XR_924927.1:n.262_277delinsGCCCGCCCTGCTGGCC
XR_924928.1:n.264_279delinsGCCCGCCCTGCTGGCC
XM_006713865.3:c.72_87delinsGCCCGCCCTGCTGGCC XP_006713928.1:p.Ala24=
XM_006713866.3:c.72_87delinsGCCCGCCCTGCTGGCC XP_006713929.1:p.Ala24=
XM_011513419.2:c.72_87delinsGCCCGCCCTGCTGGCC XP_011511721.1:p.Ala24=
XM_017007883.2:c.72_87delinsGCCCGCCCTGCTGGCC XP_016863372.1:p.Ala24=
XR_001741164.1:n.252_267delinsGCCCGCCCTGCTGGCC
XR_001741165.1:n.252_267delinsGCCCGCCCTGCTGGCC
XR_001741166.1:n.252_267delinsGCCCGCCCTGCTGGCC
XR_001741167.1:n.252_267delinsGCCCGCCCTGCTGGCC
XR_001741168.1:n.252_267delinsGCCCGCCCTGCTGGCC
XR_001741169.2:n.254_269delinsGCCCGCCCTGCTGGCC
XR_001741170.1:n.254_269delinsGCCCGCCCTGCTGGCC
XR_427473.3:n.252_267delinsGCCCGCCCTGCTGGCC
XR_427475.3:n.252_267delinsGCCCGCCCTGCTGGCC
XR_427476.3:n.252_267delinsGCCCGCCCTGCTGGCC
XR_924920.2:n.252_267delinsGCCCGCCCTGCTGGCC
XR_924921.2:n.252_267delinsGCCCGCCCTGCTGGCC
XR_924922.2:n.252_267delinsGCCCGCCCTGCTGGCC
XR_924924.2:n.252_267delinsGCCCGCCCTGCTGGCC
XR_924925.2:n.252_267delinsGCCCGCCCTGCTGGCC
XR_924926.2:n.252_267delinsGCCCGCCCTGCTGGCC
NM_153717.3:c.72_87delinsGCCCGCCCTGCTGGCC MANE Select NP_714928.1:p.Ala24=
NM_001306090.2:c.72_87delinsGCCCGCCCTGCTGGCC NP_001293019.1:p.Ala24=
NM_001306092.2:c.72_87delinsGCCCGCCCTGCTGGCC NP_001293021.1:p.Ala24=