Canonical Allele Identifier: CA2740091177

Gene: EVC CRMP1

Linked Data

• ClinVar Variation Id: 2939143
• ClinVar RCV Id: RCV003791869

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5753068_5753079del , CM000666.2:g.5753068_5753079del	GRCh38
NC_000004.11:g.5754795_5754806del , CM000666.1:g.5754795_5754806del	GRCh37
NC_000004.10:g.5805696_5805707del	NCBI36
NG_008843.1:g.46872_46883del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264956.11:c.1315+16_1315+27del (EVC) MANE Select	ENSP00000264956.6:n.1315+16_1315+27del
ENST00000264956.10:c.1315+16_1315+27del (EVC)	ENSP00000264956.6:n.1315+16_1315+27del
ENST00000506216.5:n.1648-4766_1648-4755del (CRMP1)
ENST00000509451.1:c.1315+16_1315+27del (EVC)	ENSP00000426774.1:n.1315+16_1315+27del
ENST00000514919.1:n.378+16_378+27del (EVC)
NM_001306090.1:c.1315+16_1315+27del (EVC)	NP_001293019.1:n.1315+16_1315+27del
NM_001306092.1:c.1315+16_1315+27del (EVC)	NP_001293021.1:n.1315+16_1315+27del
NM_153717.2:c.1315+16_1315+27del (EVC)	NP_714928.1:n.1315+16_1315+27del
XM_006713865.2:c.1315+16_1315+27del (EVC)	XP_006713928.1:n.1315+16_1315+27del
XM_006713866.2:c.1315+16_1315+27del (EVC)	XP_006713929.1:n.1315+16_1315+27del
XM_011513419.1:c.1315+16_1315+27del (EVC)	XP_011511721.1:n.1315+16_1315+27del
XR_427473.2:n.1505+16_1505+27del (EVC)
XR_427475.2:n.1505+16_1505+27del (EVC)
XR_427476.2:n.1505+16_1505+27del (EVC)
XR_924920.1:n.1505+16_1505+27del (EVC)
XR_924921.1:n.1505+16_1505+27del (EVC)
XR_924922.1:n.1505+16_1505+27del (EVC)
XR_924923.1:n.1505+16_1505+27del (EVC)
XR_924924.1:n.1505+16_1505+27del (EVC)
XR_924925.1:n.1505+16_1505+27del (EVC)
XR_924926.1:n.1505+16_1505+27del (EVC)
XR_924927.1:n.1505+16_1505+27del (EVC)
XR_924928.1:n.1507+16_1507+27del (EVC)
XM_006713865.3:c.1315+16_1315+27del (EVC)	XP_006713928.1:n.1315+16_1315+27del
XM_006713866.3:c.1315+16_1315+27del (EVC)	XP_006713929.1:n.1315+16_1315+27del
XM_011513419.2:c.1315+16_1315+27del (EVC)	XP_011511721.1:n.1315+16_1315+27del
XM_017007883.2:c.1315+16_1315+27del (EVC)	XP_016863372.1:n.1315+16_1315+27del
XR_001741164.1:n.1495+16_1495+27del (EVC)
XR_001741165.1:n.1495+16_1495+27del (EVC)
XR_001741166.1:n.1495+16_1495+27del (EVC)
XR_001741167.1:n.1495+16_1495+27del (EVC)
XR_001741168.1:n.1495+16_1495+27del (EVC)
XR_001741169.2:n.1359+16_1359+27del (EVC)
XR_001741170.1:n.1497+16_1497+27del (EVC)
XR_001741171.1:n.800+16_800+27del (EVC)
XR_427473.3:n.1495+16_1495+27del (EVC)
XR_427475.3:n.1495+16_1495+27del (EVC)
XR_427476.3:n.1495+16_1495+27del (EVC)
XR_924920.2:n.1495+16_1495+27del (EVC)
XR_924921.2:n.1495+16_1495+27del (EVC)
XR_924922.2:n.1495+16_1495+27del (EVC)
XR_924924.2:n.1495+16_1495+27del (EVC)
XR_924925.2:n.1495+16_1495+27del (EVC)
XR_924926.2:n.1495+16_1495+27del (EVC)
NM_153717.3:c.1315+16_1315+27del (EVC) MANE Select	NP_714928.1:n.1315+16_1315+27del
NM_001306090.2:c.1315+16_1315+27del (EVC)	NP_001293019.1:n.1315+16_1315+27del
NM_001306092.2:c.1315+16_1315+27del (EVC)	NP_001293021.1:n.1315+16_1315+27del