Canonical Allele Identifier: CA112131234

Gene: CYP4V2

Linked Data

• dbSNP Id: rs777541889
• MyVariant Identifiers: chr4:g.187125950_187125951insT (hg19) ; chr4:g.186204796_186204797insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204797dup , CM000666.2:g.186204797dup	GRCh38
NC_000004.11:g.187125951dup , CM000666.1:g.187125951dup	GRCh37
NC_000004.10:g.187362945dup	NCBI36
NG_007965.1:g.18278dup
NG_012095.2:g.819dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-403dup MANE Select	ENSP00000368079.4:n.988-403dup
ENST00000378802.4:c.988-403dup	ENSP00000368079.4:n.988-403dup
ENST00000507209.5:n.5283dup
ENST00000513354.5:n.77+340dup
NM_207352.3:c.988-403dup	NP_997235.3:n.988-403dup
XM_005262935.2:c.988-403dup	XP_005262992.1:n.988-403dup
XM_006714184.2:c.592-403dup	XP_006714247.1:n.592-403dup
XM_005262935.4:c.988-403dup	XP_005262992.1:n.988-403dup
XM_017008037.1:c.592-403dup	XP_016863526.1:n.592-403dup
NM_207352.4:c.988-403dup MANE Select	NP_997235.3:n.988-403dup