Canonical Allele Identifier: CA1058845726
Gene: EVC HGNC NCBI

Linked Data

dbSNP Id: rs1379620550
gnomAD v3: 4-5711258-A-C
gnomAD v4: 4-5711258-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.5711258A>C , CM000666.2:g.5711258A>C GRCh38
NC_000004.11:g.5712985A>C , CM000666.1:g.5712985A>C GRCh37
NC_000004.10:g.5763886A>C NCBI36
NG_008843.1:g.5062A>C
NG_015821.1:g.3291T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264956.11:c.-123A>C MANE Select ENSP00000264956.6:n.-123A>C
ENST00000264956.10:c.-123A>C ENSP00000264956.6:n.-123A>C
ENST00000509451.1:c.-123A>C ENSP00000426774.1:n.-123A>C
NM_001306090.1:c.-123A>C NP_001293019.1:n.-123A>C
NM_001306092.1:c.-123A>C NP_001293021.1:n.-123A>C
NM_153717.2:c.-123A>C NP_714928.1:n.-123A>C
XM_006713865.2:c.-123A>C XP_006713928.1:n.-123A>C
XM_006713866.2:c.-123A>C XP_006713929.1:n.-123A>C
XM_011513419.1:c.-123A>C XP_011511721.1:n.-123A>C
XR_427473.2:n.68A>C
XR_427475.2:n.68A>C
XR_427476.2:n.68A>C
XR_924920.1:n.68A>C
XR_924921.1:n.68A>C
XR_924922.1:n.68A>C
XR_924923.1:n.68A>C
XR_924924.1:n.68A>C
XR_924925.1:n.68A>C
XR_924926.1:n.68A>C
XR_924927.1:n.68A>C
XR_924928.1:n.70A>C
XM_006713865.3:c.-123A>C XP_006713928.1:n.-123A>C
XM_006713866.3:c.-123A>C XP_006713929.1:n.-123A>C
XM_011513419.2:c.-123A>C XP_011511721.1:n.-123A>C
XM_017007883.2:c.-123A>C XP_016863372.1:n.-123A>C
XR_001741164.1:n.58A>C
XR_001741165.1:n.58A>C
XR_001741166.1:n.58A>C
XR_001741167.1:n.58A>C
XR_001741168.1:n.58A>C
XR_001741169.2:n.60A>C
XR_001741170.1:n.60A>C
XR_427473.3:n.58A>C
XR_427475.3:n.58A>C
XR_427476.3:n.58A>C
XR_924920.2:n.58A>C
XR_924921.2:n.58A>C
XR_924922.2:n.58A>C
XR_924924.2:n.58A>C
XR_924925.2:n.58A>C
XR_924926.2:n.58A>C
NM_153717.3:c.-123A>C MANE Select NP_714928.1:n.-123A>C
NM_001306090.2:c.-123A>C NP_001293019.1:n.-123A>C
NM_001306092.2:c.-123A>C NP_001293021.1:n.-123A>C