Canonical Allele Identifier: CA1519915045
Gene: CYP4V2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194545_186194548delinsTGCC , CM000666.2:g.186194545_186194548delinsTGCC GRCh38
NC_000004.11:g.187115699_187115702delinsTGCC , CM000666.1:g.187115699_187115702delinsTGCC GRCh37
NC_000004.10:g.187352693_187352696delinsTGCC NCBI36
NG_007965.1:g.8026_8029delinsTGCC

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.260_263delinsTGCC MANE Select ENSP00000368079.4:p.Met87=
ENST00000378802.4:c.260_263delinsTGCC ENSP00000368079.4:p.Met87=
NM_207352.3:c.260_263delinsTGCC NP_997235.3:p.Met87=
XM_005262935.2:c.260_263delinsTGCC XP_005262992.1:p.Met87=
XM_006714184.2:c.-51_-48delinsTGCC XP_006714247.1:n.-51_-48delinsTGCC
XM_005262935.4:c.260_263delinsTGCC XP_005262992.1:p.Met87=
XM_017008037.1:c.-51_-48delinsTGCC XP_016863526.1:n.-51_-48delinsTGCC
NM_207352.4:c.260_263delinsTGCC MANE Select NP_997235.3:p.Met87=
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