Canonical Allele Identifier: CA2672892950
Gene: CYP4V2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186191984_186192004dup , CM000666.2:g.186191984_186192004dup GRCh38
NC_000004.11:g.187113138_187113158dup , CM000666.1:g.187113138_187113158dup GRCh37
NC_000004.10:g.187350132_187350152dup NCBI36
NG_007965.1:g.5465_5485dup

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.161_181dup MANE Select ENSP00000368079.4:p.Val60_Gly61insAlaArgA...
ENST00000378802.4:c.161_181dup ENSP00000368079.4:p.Val60_Gly61insAlaArgA...
NM_207352.3:c.161_181dup NP_997235.3:p.Val60_Gly61insAlaArgAlaTyrP...
XM_005262935.2:c.161_181dup XP_005262992.1:p.Val60_Gly61insAlaArgAlaT...
XM_005262935.4:c.161_181dup XP_005262992.1:p.Val60_Gly61insAlaArgAlaT...
XM_017008037.1:c.-150_-130dup XP_016863526.1:n.-150_-130dup
NM_207352.4:c.161_181dup MANE Select NP_997235.3:p.Val60_Gly61insAlaArgAlaTyrP...