Canonical Allele Identifier: CA549401791

Gene: EVC CRMP1

Linked Data

• dbSNP Id: rs5855888
• gnomAD v2: 4-5757932-G-GAA
• gnomAD v3: 4-5756205-G-GAA
• gnomAD v4: 4-5756205-G-GAA
• MyVariant Identifiers: chr4:g.5757933_5757934insAA (hg19) ; chr4:g.5757932_5757933insAA (hg19) ; chr4:g.5756206_5756207insAA (hg38) ; chr4:g.5756205_5756206insAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5756219_5756220dup , CM000666.2:g.5756219_5756220dup	GRCh38
NC_000004.11:g.5757946_5757947dup , CM000666.1:g.5757946_5757947dup	GRCh37
NC_000004.10:g.5808847_5808848dup	NCBI36
NG_008843.1:g.50023_50024dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264956.11:c.1465-45_1465-44dup (EVC) MANE Select	ENSP00000264956.6:n.1465-45_1465-44dup
ENST00000264956.10:c.1465-45_1465-44dup (EVC)	ENSP00000264956.6:n.1465-45_1465-44dup
ENST00000506216.5:n.1648-7895_1648-7894dup (CRMP1)
ENST00000509451.1:c.1465-45_1465-44dup (EVC)	ENSP00000426774.1:n.1465-45_1465-44dup
NM_001306090.1:c.1465-45_1465-44dup (EVC)	NP_001293019.1:n.1465-45_1465-44dup
NM_001306092.1:c.1465-45_1465-44dup (EVC)	NP_001293021.1:n.1465-45_1465-44dup
NM_153717.2:c.1465-45_1465-44dup (EVC)	NP_714928.1:n.1465-45_1465-44dup
XM_006713865.2:c.1465-45_1465-44dup (EVC)	XP_006713928.1:n.1465-45_1465-44dup
XM_006713866.2:c.1465-45_1465-44dup (EVC)	XP_006713929.1:n.1465-45_1465-44dup
XM_011513419.1:c.1465-45_1465-44dup (EVC)	XP_011511721.1:n.1465-45_1465-44dup
XR_427473.2:n.1655-45_1655-44dup (EVC)
XR_427475.2:n.1655-45_1655-44dup (EVC)
XR_427476.2:n.1655-45_1655-44dup (EVC)
XR_924920.1:n.1655-45_1655-44dup (EVC)
XR_924921.1:n.1655-45_1655-44dup (EVC)
XR_924922.1:n.1655-45_1655-44dup (EVC)
XR_924923.1:n.1655-45_1655-44dup (EVC)
XR_924924.1:n.1655-45_1655-44dup (EVC)
XR_924925.1:n.1655-45_1655-44dup (EVC)
XR_924926.1:n.1655-45_1655-44dup (EVC)
XR_924927.1:n.1655-45_1655-44dup (EVC)
XR_924928.1:n.1657-45_1657-44dup (EVC)
XM_006713865.3:c.1465-45_1465-44dup (EVC)	XP_006713928.1:n.1465-45_1465-44dup
XM_006713866.3:c.1465-45_1465-44dup (EVC)	XP_006713929.1:n.1465-45_1465-44dup
XM_011513419.2:c.1465-45_1465-44dup (EVC)	XP_011511721.1:n.1465-45_1465-44dup
XM_017007883.2:c.1465-45_1465-44dup (EVC)	XP_016863372.1:n.1465-45_1465-44dup
XR_001741164.1:n.1645-45_1645-44dup (EVC)
XR_001741165.1:n.1645-45_1645-44dup (EVC)
XR_001741166.1:n.1645-45_1645-44dup (EVC)
XR_001741167.1:n.1645-45_1645-44dup (EVC)
XR_001741168.1:n.1645-45_1645-44dup (EVC)
XR_001741169.2:n.1509-45_1509-44dup (EVC)
XR_001741170.1:n.1647-45_1647-44dup (EVC)
XR_001741171.1:n.950-45_950-44dup (EVC)
XR_427473.3:n.1645-45_1645-44dup (EVC)
XR_427475.3:n.1645-45_1645-44dup (EVC)
XR_427476.3:n.1645-45_1645-44dup (EVC)
XR_924920.2:n.1645-45_1645-44dup (EVC)
XR_924921.2:n.1645-45_1645-44dup (EVC)
XR_924922.2:n.1645-45_1645-44dup (EVC)
XR_924924.2:n.1645-45_1645-44dup (EVC)
XR_924925.2:n.1645-45_1645-44dup (EVC)
XR_924926.2:n.1645-45_1645-44dup (EVC)
NM_153717.3:c.1465-45_1465-44dup (EVC) MANE Select	NP_714928.1:n.1465-45_1465-44dup
NM_001306090.2:c.1465-45_1465-44dup (EVC)	NP_001293019.1:n.1465-45_1465-44dup
NM_001306092.2:c.1465-45_1465-44dup (EVC)	NP_001293021.1:n.1465-45_1465-44dup