Canonical Allele Identifier: CA792329251

Gene: CYP4V2 KLKB1

Linked Data

• dbSNP Id: rs1299817976
• MyVariant Identifiers: chr4:g.187131588_187131589insT (hg19) ; chr4:g.186210434_186210435insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186210435dup , CM000666.2:g.186210435dup	GRCh38
NC_000004.11:g.187131589dup , CM000666.1:g.187131589dup	GRCh37
NC_000004.10:g.187368583dup	NCBI36
NG_007965.1:g.23916dup
NG_012095.2:g.6457dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1406-34dup (CYP4V2) MANE Select	ENSP00000368079.4:n.1406-34dup
ENST00000378802.4:c.1406-34dup (CYP4V2)	ENSP00000368079.4:n.1406-34dup
ENST00000502665.1:n.641-34dup (CYP4V2)
ENST00000507209.5:n.6104-34dup (CYP4V2)
ENST00000511608.5:c.201+1163dup (KLKB1)
ENST00000513354.5:n.496-34dup (CYP4V2)
NM_207352.3:c.1406-34dup (CYP4V2)	NP_997235.3:n.1406-34dup
XM_005262935.2:c.1403-34dup (CYP4V2)	XP_005262992.1:n.1403-34dup
XM_006714184.2:c.1010-34dup (CYP4V2)	XP_006714247.1:n.1010-34dup
XM_005262935.4:c.1403-34dup (CYP4V2)	XP_005262992.1:n.1403-34dup
XM_017008037.1:c.1010-34dup (CYP4V2)	XP_016863526.1:n.1010-34dup
NM_207352.4:c.1406-34dup (CYP4V2) MANE Select	NP_997235.3:n.1406-34dup