Canonical Allele Identifier: CA1435493861

Gene: EVC CRMP1

Linked Data

• dbSNP Id: rs1731146638

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5756224_5756226del , CM000666.2:g.5756224_5756226del	GRCh38
NC_000004.11:g.5757951_5757953del , CM000666.1:g.5757951_5757953del	GRCh37
NC_000004.10:g.5808852_5808854del	NCBI36
NG_008843.1:g.50028_50030del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264956.11:c.1465-40_1465-38del (EVC) MANE Select	ENSP00000264956.6:n.1465-40_1465-38del
ENST00000264956.10:c.1465-40_1465-38del (EVC)	ENSP00000264956.6:n.1465-40_1465-38del
ENST00000506216.5:n.1648-7913_1648-7911del (CRMP1)
ENST00000509451.1:c.1465-40_1465-38del (EVC)	ENSP00000426774.1:n.1465-40_1465-38del
NM_001306090.1:c.1465-40_1465-38del (EVC)	NP_001293019.1:n.1465-40_1465-38del
NM_001306092.1:c.1465-40_1465-38del (EVC)	NP_001293021.1:n.1465-40_1465-38del
NM_153717.2:c.1465-40_1465-38del (EVC)	NP_714928.1:n.1465-40_1465-38del
XM_006713865.2:c.1465-40_1465-38del (EVC)	XP_006713928.1:n.1465-40_1465-38del
XM_006713866.2:c.1465-40_1465-38del (EVC)	XP_006713929.1:n.1465-40_1465-38del
XM_011513419.1:c.1465-40_1465-38del (EVC)	XP_011511721.1:n.1465-40_1465-38del
XR_427473.2:n.1655-40_1655-38del (EVC)
XR_427475.2:n.1655-40_1655-38del (EVC)
XR_427476.2:n.1655-40_1655-38del (EVC)
XR_924920.1:n.1655-40_1655-38del (EVC)
XR_924921.1:n.1655-40_1655-38del (EVC)
XR_924922.1:n.1655-40_1655-38del (EVC)
XR_924923.1:n.1655-40_1655-38del (EVC)
XR_924924.1:n.1655-40_1655-38del (EVC)
XR_924925.1:n.1655-40_1655-38del (EVC)
XR_924926.1:n.1655-40_1655-38del (EVC)
XR_924927.1:n.1655-40_1655-38del (EVC)
XR_924928.1:n.1657-40_1657-38del (EVC)
XM_006713865.3:c.1465-40_1465-38del (EVC)	XP_006713928.1:n.1465-40_1465-38del
XM_006713866.3:c.1465-40_1465-38del (EVC)	XP_006713929.1:n.1465-40_1465-38del
XM_011513419.2:c.1465-40_1465-38del (EVC)	XP_011511721.1:n.1465-40_1465-38del
XM_017007883.2:c.1465-40_1465-38del (EVC)	XP_016863372.1:n.1465-40_1465-38del
XR_001741164.1:n.1645-40_1645-38del (EVC)
XR_001741165.1:n.1645-40_1645-38del (EVC)
XR_001741166.1:n.1645-40_1645-38del (EVC)
XR_001741167.1:n.1645-40_1645-38del (EVC)
XR_001741168.1:n.1645-40_1645-38del (EVC)
XR_001741169.2:n.1509-40_1509-38del (EVC)
XR_001741170.1:n.1647-40_1647-38del (EVC)
XR_001741171.1:n.950-40_950-38del (EVC)
XR_427473.3:n.1645-40_1645-38del (EVC)
XR_427475.3:n.1645-40_1645-38del (EVC)
XR_427476.3:n.1645-40_1645-38del (EVC)
XR_924920.2:n.1645-40_1645-38del (EVC)
XR_924921.2:n.1645-40_1645-38del (EVC)
XR_924922.2:n.1645-40_1645-38del (EVC)
XR_924924.2:n.1645-40_1645-38del (EVC)
XR_924925.2:n.1645-40_1645-38del (EVC)
XR_924926.2:n.1645-40_1645-38del (EVC)
NM_153717.3:c.1465-40_1465-38del (EVC) MANE Select	NP_714928.1:n.1465-40_1465-38del
NM_001306090.2:c.1465-40_1465-38del (EVC)	NP_001293019.1:n.1465-40_1465-38del
NM_001306092.2:c.1465-40_1465-38del (EVC)	NP_001293021.1:n.1465-40_1465-38del