Canonical Allele Identifier: CA2838308716
Gene: CYP4V2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194497dup , CM000666.2:g.186194497dup GRCh38
NC_000004.11:g.187115651dup , CM000666.1:g.187115651dup GRCh37
NC_000004.10:g.187352645dup NCBI36
NG_007965.1:g.7978dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.215-3dup MANE Select ENSP00000368079.4:n.215-3dup
ENST00000378802.4:c.215-3dup ENSP00000368079.4:n.215-3dup
NM_207352.3:c.215-3dup NP_997235.3:n.215-3dup
XM_005262935.2:c.215-3dup XP_005262992.1:n.215-3dup
XM_005262935.4:c.215-3dup XP_005262992.1:n.215-3dup
XM_017008037.1:c.-96-3dup XP_016863526.1:n.-96-3dup
NM_207352.4:c.215-3dup MANE Select NP_997235.3:n.215-3dup
Search 100 bp 5'
Search 100 bp 3'