Canonical Allele Identifier: CA1435522893

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.5808295C= , CM000666.2:g.5808295C= GRCh38
NC_000004.11:g.5810022C= , CM000666.1:g.5810022C= GRCh37
NC_000004.10:g.5860923C= NCBI36
NG_008843.1:g.102099C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264956.11:c.2656C= (EVC) MANE Select ENSP00000264956.6:p.Leu886=
ENST00000264956.10:c.2656C= (EVC) ENSP00000264956.6:p.Leu886=
ENST00000506216.5:n.1647+17199G= (CRMP1)
NM_001306090.1:c.2656C= (EVC) NP_001293019.1:p.Leu886=
NM_153717.2:c.2656C= (EVC) NP_714928.1:p.Leu886=
XM_006713865.2:c.2656C= (EVC) XP_006713928.1:p.Leu886=
XM_006713866.2:c.2656C= (EVC) XP_006713929.1:p.Leu886=
XR_427473.2:n.2846C= (EVC)
XR_427475.2:n.2846C= (EVC)
XR_427476.2:n.2846C= (EVC)
XR_924920.1:n.2846C= (EVC)
XR_924921.1:n.2846C= (EVC)
XR_924922.1:n.2846C= (EVC)
XR_924923.1:n.2846C= (EVC)
XR_924924.1:n.2846C= (EVC)
XR_924925.1:n.2846C= (EVC)
XR_924926.1:n.2846C= (EVC)
XR_924927.1:n.2846C= (EVC)
XM_006713865.3:c.2656C= (EVC) XP_006713928.1:p.Leu886=
XM_006713866.3:c.2656C= (EVC) XP_006713929.1:p.Leu886=
XR_001741164.1:n.2836C= (EVC)
XR_001741165.1:n.2836C= (EVC)
XR_001741166.1:n.2836C= (EVC)
XR_001741167.1:n.2836C= (EVC)
XR_001741168.1:n.2836C= (EVC)
XR_001741169.2:n.2700C= (EVC)
XR_001741170.1:n.2921C= (EVC)
XR_001741171.1:n.2141C= (EVC)
XR_427473.3:n.2836C= (EVC)
XR_427475.3:n.2836C= (EVC)
XR_427476.3:n.2836C= (EVC)
XR_924920.2:n.2836C= (EVC)
XR_924921.2:n.2836C= (EVC)
XR_924922.2:n.2836C= (EVC)
XR_924924.2:n.2836C= (EVC)
XR_924925.2:n.2836C= (EVC)
XR_924926.2:n.2836C= (EVC)
NM_153717.3:c.2656C= (EVC) MANE Select NP_714928.1:p.Leu886=
NM_001306090.2:c.2656C= (EVC) NP_001293019.1:p.Leu886=