Canonical Allele Identifier: CA1519919356
Gene: CYP4V2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186197562_186197567delinsCAAAGT , CM000666.2:g.186197562_186197567delinsCAAAGT GRCh38
NC_000004.11:g.187118716_187118721delinsCAAAGT , CM000666.1:g.187118716_187118721delinsCAAAGT GRCh37
NC_000004.10:g.187355710_187355715delinsCAAAGT NCBI36
NG_007965.1:g.11043_11048delinsCAAAGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.634_639delinsCAAAGT MANE Select ENSP00000368079.4:p.Gln212=
ENST00000378802.4:c.634_639delinsCAAAGT ENSP00000368079.4:p.Gln212=
ENST00000507209.5:n.1475_1480delinsCAAAGT
NM_207352.3:c.634_639delinsCAAAGT NP_997235.3:p.Gln212=
XM_005262935.2:c.634_639delinsCAAAGT XP_005262992.1:p.Gln212=
XM_006714184.2:c.238_243delinsCAAAGT XP_006714247.1:p.Gln80=
XM_005262935.4:c.634_639delinsCAAAGT XP_005262992.1:p.Gln212=
XM_017008037.1:c.238_243delinsCAAAGT XP_016863526.1:p.Gln80=
NM_207352.4:c.634_639delinsCAAAGT MANE Select NP_997235.3:p.Gln212=
Search 100 bp 5'
Search 100 bp 3'