Canonical Allele Identifier: CA2588340364

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.5756205_5756206delinsGA , CM000666.2:g.5756205_5756206delinsGA GRCh38
NC_000004.11:g.5757932_5757933delinsGA , CM000666.1:g.5757932_5757933delinsGA GRCh37
NC_000004.10:g.5808833_5808834delinsGA NCBI36
NG_008843.1:g.50009_50010delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000264956.11:c.1465-59_1465-58delinsGA (EVC) MANE Select ENSP00000264956.6:n.1465-59_1465-58delinsGA
ENST00000264956.10:c.1465-59_1465-58delinsGA (EVC) ENSP00000264956.6:n.1465-59_1465-58delinsGA
ENST00000506216.5:n.1648-7894_1648-7893delinsTC (CRMP1)
ENST00000509451.1:c.1465-59_1465-58delinsGA (EVC) ENSP00000426774.1:n.1465-59_1465-58delinsGA
NM_001306090.1:c.1465-59_1465-58delinsGA (EVC) NP_001293019.1:n.1465-59_1465-58delinsGA
NM_001306092.1:c.1465-59_1465-58delinsGA (EVC) NP_001293021.1:n.1465-59_1465-58delinsGA
NM_153717.2:c.1465-59_1465-58delinsGA (EVC) NP_714928.1:n.1465-59_1465-58delinsGA
XM_006713865.2:c.1465-59_1465-58delinsGA (EVC) XP_006713928.1:n.1465-59_1465-58delinsGA
XM_006713866.2:c.1465-59_1465-58delinsGA (EVC) XP_006713929.1:n.1465-59_1465-58delinsGA
XM_011513419.1:c.1465-59_1465-58delinsGA (EVC) XP_011511721.1:n.1465-59_1465-58delinsGA
XR_427473.2:n.1655-59_1655-58delinsGA (EVC)
XR_427475.2:n.1655-59_1655-58delinsGA (EVC)
XR_427476.2:n.1655-59_1655-58delinsGA (EVC)
XR_924920.1:n.1655-59_1655-58delinsGA (EVC)
XR_924921.1:n.1655-59_1655-58delinsGA (EVC)
XR_924922.1:n.1655-59_1655-58delinsGA (EVC)
XR_924923.1:n.1655-59_1655-58delinsGA (EVC)
XR_924924.1:n.1655-59_1655-58delinsGA (EVC)
XR_924925.1:n.1655-59_1655-58delinsGA (EVC)
XR_924926.1:n.1655-59_1655-58delinsGA (EVC)
XR_924927.1:n.1655-59_1655-58delinsGA (EVC)
XR_924928.1:n.1657-59_1657-58delinsGA (EVC)
XM_006713865.3:c.1465-59_1465-58delinsGA (EVC) XP_006713928.1:n.1465-59_1465-58delinsGA
XM_006713866.3:c.1465-59_1465-58delinsGA (EVC) XP_006713929.1:n.1465-59_1465-58delinsGA
XM_011513419.2:c.1465-59_1465-58delinsGA (EVC) XP_011511721.1:n.1465-59_1465-58delinsGA
XM_017007883.2:c.1465-59_1465-58delinsGA (EVC) XP_016863372.1:n.1465-59_1465-58delinsGA
XR_001741164.1:n.1645-59_1645-58delinsGA (EVC)
XR_001741165.1:n.1645-59_1645-58delinsGA (EVC)
XR_001741166.1:n.1645-59_1645-58delinsGA (EVC)
XR_001741167.1:n.1645-59_1645-58delinsGA (EVC)
XR_001741168.1:n.1645-59_1645-58delinsGA (EVC)
XR_001741169.2:n.1509-59_1509-58delinsGA (EVC)
XR_001741170.1:n.1647-59_1647-58delinsGA (EVC)
XR_001741171.1:n.950-59_950-58delinsGA (EVC)
XR_427473.3:n.1645-59_1645-58delinsGA (EVC)
XR_427475.3:n.1645-59_1645-58delinsGA (EVC)
XR_427476.3:n.1645-59_1645-58delinsGA (EVC)
XR_924920.2:n.1645-59_1645-58delinsGA (EVC)
XR_924921.2:n.1645-59_1645-58delinsGA (EVC)
XR_924922.2:n.1645-59_1645-58delinsGA (EVC)
XR_924924.2:n.1645-59_1645-58delinsGA (EVC)
XR_924925.2:n.1645-59_1645-58delinsGA (EVC)
XR_924926.2:n.1645-59_1645-58delinsGA (EVC)
NM_153717.3:c.1465-59_1465-58delinsGA (EVC) MANE Select NP_714928.1:n.1465-59_1465-58delinsGA
NM_001306090.2:c.1465-59_1465-58delinsGA (EVC) NP_001293019.1:n.1465-59_1465-58delinsGA
NM_001306092.2:c.1465-59_1465-58delinsGA (EVC) NP_001293021.1:n.1465-59_1465-58delinsGA