Canonical Allele Identifier: CA386646109

Gene: MVK

Linked Data

• ClinVar Variation Id: 2942860
• ClinVar RCV Id: RCV003808026
• dbSNP Id: rs752578165
• MyVariant Identifiers: chr12:g.110019247G>T (hg19) ; chr12:g.109581442G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109581442G>T , CM000674.2:g.109581442G>T	GRCh38
NC_000012.11:g.110019247G>T , CM000674.1:g.110019247G>T	GRCh37
NC_000012.10:g.108503630G>T	NCBI36
NG_007702.1:g.12748G>T , LRG_156:g.12748G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539696.6:c.-92+7569G>T	ENSP00000439134.1:n.-92+7569G>T
ENST00000546277.6:c.419G>T	ENSP00000438153.2:p.Gly140Val
ENST00000636529.2:n.79-4580G>T
ENST00000697195.1:c.*183G>T	ENSP00000513181.1:n.*183G>T
ENST00000697196.1:c.419G>T	ENSP00000513182.1:p.Gly140Val
ENST00000228510.8:c.419G>T MANE Select	ENSP00000228510.3:p.Gly140Val
ENST00000636529.1:c.65-4580G>T
ENST00000636996.1:c.267G>T
ENST00000228510.7:c.419G>T	ENSP00000228510.3:p.Gly140Val
ENST00000392727.7:c.371+1496G>T	ENSP00000376487.3:n.371+1496G>T
ENST00000447878.6:c.227-4580G>T	ENSP00000415555.2:n.227-4580G>T
ENST00000535044.1:n.472-4580G>T
ENST00000537237.5:c.*183G>T	ENSP00000445382.1:n.*183G>T
ENST00000539335.5:c.419G>T	ENSP00000440379.1:p.Gly140Val
ENST00000539575.4:c.419G>T	ENSP00000443551.2:p.Gly140Val
ENST00000539696.5:c.-92+7569G>T	ENSP00000439134.1:n.-92+7569G>T
ENST00000545774.5:c.227-4580G>T	ENSP00000443978.1:n.227-4580G>T
ENST00000546277.5:c.419G>T	ENSP00000438153.1:p.Gly140Val
ENST00000625889.2:c.371+1496G>T	ENSP00000486846.1:n.371+1496G>T
ENST00000629016.2:c.227-4580G>T	ENSP00000486804.1:n.227-4580G>T
NM_000431.3:c.419G>T	NP_000422.1:p.Gly140Val
NM_001114185.2:c.419G>T	NP_001107657.1:p.Gly140Val
NM_001301182.1:c.371+1496G>T	NP_001288111.1:n.371+1496G>T
XM_011538372.1:c.419G>T	XP_011536674.1:p.Gly140Val
XM_017019313.2:c.371+1496G>T	XP_016874802.1:n.371+1496G>T
XM_017019314.1:c.419G>T	XP_016874803.1:p.Gly140Val
XM_024448982.1:c.419G>T	XP_024304750.1:p.Gly140Val
NM_000431.4:c.419G>T MANE Select	NP_000422.1:p.Gly140Val
NM_001114185.3:c.419G>T	NP_001107657.1:p.Gly140Val
NM_001301182.2:c.371+1496G>T	NP_001288111.1:n.371+1496G>T