Canonical Allele Identifier: CA386651522

Gene: MVK

Linked Data

• MyVariant Identifiers: chr12:g.110034381G>T (hg19) ; chr12:g.109596576G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109596576G>T , CM000674.2:g.109596576G>T	GRCh38
NC_000012.11:g.110034381G>T , CM000674.1:g.110034381G>T	GRCh37
NC_000012.10:g.108518764G>T	NCBI36
NG_007702.1:g.27882G>T , LRG_156:g.27882G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539696.6:c.347G>T	ENSP00000439134.1:p.Ter116Leu
ENST00000546277.6:c.1190G>T	ENSP00000438153.2:p.Ter397Leu
ENST00000636529.2:n.829G>T
ENST00000697195.1:c.*954G>T	ENSP00000513181.1:n.*954G>T
ENST00000697196.1:c.*363G>T	ENSP00000513182.1:n.*363G>T
ENST00000697197.1:n.3219G>T
ENST00000697198.1:n.1574G>T
ENST00000228510.8:c.1190G>T MANE Select	ENSP00000228510.3:p.Ter397Leu
ENST00000636529.1:c.815G>T
ENST00000636996.1:c.1038G>T
ENST00000228510.7:c.1190G>T	ENSP00000228510.3:p.Ter397Leu
ENST00000392727.7:c.1034G>T	ENSP00000376487.3:p.Ter345Leu
ENST00000447878.6:c.*637G>T	ENSP00000415555.2:n.*637G>T
ENST00000537237.5:c.*863G>T	ENSP00000445382.1:n.*863G>T
ENST00000539575.4:c.1190G>T	ENSP00000443551.2:p.Ter397Leu
ENST00000539696.5:c.347G>T	ENSP00000439134.1:p.Ter116Leu
ENST00000540353.1:n.3423G>T
ENST00000625889.2:c.1034G>T	ENSP00000486846.1:p.Ter345Leu
ENST00000629016.2:c.*637G>T	ENSP00000486804.1:n.*637G>T
NM_000431.3:c.1190G>T	NP_000422.1:p.Ter397Leu
NM_001114185.2:c.1190G>T	NP_001107657.1:p.Ter397Leu
NM_001301182.1:c.1034G>T	NP_001288111.1:p.Ter345Leu
XM_011538372.1:c.1190G>T	XP_011536674.1:p.Ter397Leu
XM_017019313.2:c.1034G>T	XP_016874802.1:p.Ter345Leu
XM_017019314.1:c.1190G>T	XP_016874803.1:p.Ter397Leu
NM_000431.4:c.1190G>T MANE Select	NP_000422.1:p.Ter397Leu
NM_001114185.3:c.1190G>T	NP_001107657.1:p.Ter397Leu
NM_001301182.2:c.1034G>T	NP_001288111.1:p.Ter345Leu