Canonical Allele Identifier: CA1139658435
Gene: EVC HGNC NCBI

Linked Data

ClinVar Variation Id: 940843
ClinVar RCV Id: RCV001210514
dbSNP Id: rs1723019796

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.5711533_5711596del , CM000666.2:g.5711533_5711596del GRCh38
NC_000004.11:g.5713260_5713323del , CM000666.1:g.5713260_5713323del GRCh37
NC_000004.10:g.5764161_5764224del NCBI36
NG_008843.1:g.5337_5400del
NG_015821.1:g.2960_3023del

Transcript Alleles

HGVS Amino-acid change
ENST00000264956.11:c.153_174+42del
ENST00000264956.10:c.153_174+42del
ENST00000509451.1:c.153_174+42del
NM_001306090.1:c.153_174+42del
NM_001306092.1:c.153_174+42del
NM_153717.2:c.153_174+42del
XM_006713865.2:c.153_174+42del
XM_006713866.2:c.153_174+42del
XM_011513419.1:c.153_174+42del
XR_427473.2:n.343_364+42del
XR_427475.2:n.343_364+42del
XR_427476.2:n.343_364+42del
XR_924920.1:n.343_364+42del
XR_924921.1:n.343_364+42del
XR_924922.1:n.343_364+42del
XR_924923.1:n.343_364+42del
XR_924924.1:n.343_364+42del
XR_924925.1:n.343_364+42del
XR_924926.1:n.343_364+42del
XR_924927.1:n.343_364+42del
XR_924928.1:n.345_366+42del
XM_006713865.3:c.153_174+42del
XM_006713866.3:c.153_174+42del
XM_011513419.2:c.153_174+42del
XM_017007883.2:c.153_174+42del
XR_001741164.1:n.333_354+42del
XR_001741165.1:n.333_354+42del
XR_001741166.1:n.333_354+42del
XR_001741167.1:n.333_354+42del
XR_001741168.1:n.333_354+42del
XR_001741169.2:n.335_356+42del
XR_001741170.1:n.335_356+42del
XR_427473.3:n.333_354+42del
XR_427475.3:n.333_354+42del
XR_427476.3:n.333_354+42del
XR_924920.2:n.333_354+42del
XR_924921.2:n.333_354+42del
XR_924922.2:n.333_354+42del
XR_924924.2:n.333_354+42del
XR_924925.2:n.333_354+42del
XR_924926.2:n.333_354+42del
NM_153717.3:c.153_174+42del
NM_001306090.2:c.153_174+42del
NM_001306092.2:c.153_174+42del