Canonical Allele Identifier: CA2672897238

Gene: CYP4V2

Linked Data

• gnomAD v4: 4-186197247-AGCGCGGTTCTACGACC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186197250_186197265del , CM000666.2:g.186197250_186197265del	GRCh38
NC_000004.11:g.187118404_187118419del , CM000666.1:g.187118404_187118419del	GRCh37
NC_000004.10:g.187355398_187355413del	NCBI36
NG_007965.1:g.10731_10746del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.604+120_604+135del MANE Select	ENSP00000368079.4:n.604+120_604+135del
ENST00000378802.4:c.604+120_604+135del	ENSP00000368079.4:n.604+120_604+135del
ENST00000507209.5:n.1163_1178del
NM_207352.3:c.604+120_604+135del	NP_997235.3:n.604+120_604+135del
XM_005262935.2:c.604+120_604+135del	XP_005262992.1:n.604+120_604+135del
XM_006714184.2:c.208+120_208+135del	XP_006714247.1:n.208+120_208+135del
XM_005262935.4:c.604+120_604+135del	XP_005262992.1:n.604+120_604+135del
XM_017008037.1:c.208+120_208+135del	XP_016863526.1:n.208+120_208+135del
NM_207352.4:c.604+120_604+135del MANE Select	NP_997235.3:n.604+120_604+135del