Canonical Allele Identifier: CA2062459927

Gene: MVK

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109574619G= , CM000674.2:g.109574619G=	GRCh38
NC_000012.11:g.110012424G= , CM000674.1:g.110012424G=	GRCh37
NC_000012.10:g.108496807G=	NCBI36
NG_007096.1:g.3879C=
NG_007702.1:g.5925G= , LRG_156:g.5925G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539696.6:c.-92+746G=	ENSP00000439134.1:n.-92+746G=
ENST00000546277.6:c.-14-190G=	ENSP00000438153.2:n.-14-190G=
ENST00000697195.1:c.-204G=	ENSP00000513181.1:n.-204G=
ENST00000228510.8:c.-14-190G= MANE Select	ENSP00000228510.3:n.-14-190G=
ENST00000228510.7:c.-14-190G=	ENSP00000228510.3:n.-14-190G=
ENST00000392727.7:c.-14-190G=	ENSP00000376487.3:n.-14-190G=
ENST00000447878.6:c.-14-190G=	ENSP00000415555.2:n.-14-190G=
ENST00000535044.1:n.232-190G=
ENST00000537237.5:c.-14-190G=	ENSP00000445382.1:n.-14-190G=
ENST00000539335.5:c.-5-199G=	ENSP00000440379.1:n.-5-199G=
ENST00000539696.5:c.-92+746G=	ENSP00000439134.1:n.-92+746G=
ENST00000545774.5:c.-14-190G=	ENSP00000443978.1:n.-14-190G=
ENST00000546277.5:c.-14-190G=	ENSP00000438153.1:n.-14-190G=
NM_000431.3:c.-14-190G=	NP_000422.1:n.-14-190G=
NM_001114185.2:c.-5-199G=	NP_001107657.1:n.-5-199G=
NM_001301182.1:c.-14-190G=	NP_001288111.1:n.-14-190G=
XM_011538372.1:c.-14-190G=	XP_011536674.1:n.-14-190G=
XM_017019313.2:c.-14-190G=	XP_016874802.1:n.-14-190G=
XM_017019314.1:c.-71G=	XP_016874803.1:n.-71G=
XM_024448982.1:c.-14-190G=	XP_024304750.1:n.-14-190G=
NM_000431.4:c.-14-190G= MANE Select	NP_000422.1:n.-14-190G=
NM_001114185.3:c.-5-199G=	NP_001107657.1:n.-5-199G=
NM_001301182.2:c.-14-190G=	NP_001288111.1:n.-14-190G=