Canonical Allele Identifier: CA356160669
Community Standard Title: NM_153717.3(EVC):c.1607A>T (p.Asp536Val)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.5783595A>T , CM000666.2:g.5783595A>T GRCh38
NC_000004.11:g.5785322A>T , CM000666.1:g.5785322A>T GRCh37
NC_000004.10:g.5836223A>T NCBI36
NG_008843.1:g.77399A>T

Transcript Alleles

HGVS Amino-acid Change
NM_153717.3:c.1607A>T (EVC) MANE Select NP_714928.1:p.Asp536Val
ENST00000264956.11:c.1607A>T (EVC) MANE Select ENSP00000264956.6:p.Asp536Val
NM_001306090.1:c.1607A>T (EVC) NP_001293019.1:p.Asp536Val
NM_001306090.2:c.1607A>T (EVC) NP_001293019.1:p.Asp536Val
NM_153717.2:c.1607A>T (EVC) NP_714928.1:p.Asp536Val
ENST00000264956.10:c.1607A>T (EVC) ENSP00000264956.6:p.Asp536Val
ENST00000506216.5:n.1648-35283T>A (CRMP1)
XM_006713865.2:c.1607A>T (EVC) XP_006713928.1:p.Asp536Val
XM_006713865.3:c.1607A>T (EVC) XP_006713928.1:p.Asp536Val
XM_006713866.2:c.1607A>T (EVC) XP_006713929.1:p.Asp536Val
XM_006713866.3:c.1607A>T (EVC) XP_006713929.1:p.Asp536Val
XM_011513419.1:c.1607A>T (EVC) XP_011511721.1:p.Asp536Val
XM_011513419.2:c.1607A>T (EVC) XP_011511721.1:p.Asp536Val
XR_001741164.1:n.1787A>T (EVC)
XR_001741165.1:n.1787A>T (EVC)
XR_001741166.1:n.1787A>T (EVC)
XR_001741167.1:n.1787A>T (EVC)
XR_001741168.1:n.1787A>T (EVC)
XR_001741169.2:n.1651A>T (EVC)
XR_001741170.1:n.1789A>T (EVC)
XR_001741171.1:n.1092A>T (EVC)
XR_427473.2:n.1797A>T (EVC)
XR_427473.3:n.1787A>T (EVC)
XR_427475.2:n.1797A>T (EVC)
XR_427475.3:n.1787A>T (EVC)
XR_427476.2:n.1797A>T (EVC)
XR_427476.3:n.1787A>T (EVC)
XR_924920.1:n.1797A>T (EVC)
XR_924920.2:n.1787A>T (EVC)
XR_924921.1:n.1797A>T (EVC)
XR_924921.2:n.1787A>T (EVC)
XR_924922.1:n.1797A>T (EVC)
XR_924922.2:n.1787A>T (EVC)
XR_924923.1:n.1797A>T (EVC)
XR_924924.1:n.1797A>T (EVC)
XR_924924.2:n.1787A>T (EVC)
XR_924925.1:n.1797A>T (EVC)
XR_924925.2:n.1787A>T (EVC)
XR_924926.1:n.1797A>T (EVC)
XR_924926.2:n.1787A>T (EVC)
XR_924927.1:n.1797A>T (EVC)
XR_924928.1:n.1799A>T (EVC)