Canonical Allele Identifier: CA6779245

Gene: MVK

Linked Data

• dbSNP Id: rs769506953
• ExAC: 12:110019178 T / G
• gnomAD v2: 12-110019178-T-G
• gnomAD v4: 12-109581373-T-G
• MyVariant Identifiers: chr12:g.110019178T>G (hg19) ; chr12:g.109581373T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109581373T>G , CM000674.2:g.109581373T>G	GRCh38
NC_000012.11:g.110019178T>G , CM000674.1:g.110019178T>G	GRCh37
NC_000012.10:g.108503561T>G	NCBI36
NG_007702.1:g.12679T>G , LRG_156:g.12679T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000539696.6:c.-92+7500T>G	ENSP00000439134.1:n.-92+7500T>G
ENST00000546277.6:c.372-22T>G	ENSP00000438153.2:n.372-22T>G
ENST00000636529.2:n.79-4649T>G
ENST00000697195.1:c.*136-22T>G	ENSP00000513181.1:n.*136-22T>G
ENST00000697196.1:c.372-22T>G	ENSP00000513182.1:n.372-22T>G
ENST00000228510.8:c.372-22T>G MANE Select	ENSP00000228510.3:n.372-22T>G
ENST00000636529.1:c.65-4649T>G
ENST00000636996.1:c.220-22T>G
ENST00000228510.7:c.372-22T>G	ENSP00000228510.3:n.372-22T>G
ENST00000392727.7:c.371+1427T>G	ENSP00000376487.3:n.371+1427T>G
ENST00000447878.6:c.227-4649T>G	ENSP00000415555.2:n.227-4649T>G
ENST00000535044.1:n.472-4649T>G
ENST00000537237.5:c.*136-22T>G	ENSP00000445382.1:n.*136-22T>G
ENST00000539335.5:c.372-22T>G	ENSP00000440379.1:n.372-22T>G
ENST00000539575.4:c.372-22T>G	ENSP00000443551.2:n.372-22T>G
ENST00000539696.5:c.-92+7500T>G	ENSP00000439134.1:n.-92+7500T>G
ENST00000545774.5:c.227-4649T>G	ENSP00000443978.1:n.227-4649T>G
ENST00000546277.5:c.372-22T>G	ENSP00000438153.1:n.372-22T>G
ENST00000625889.2:c.371+1427T>G	ENSP00000486846.1:n.371+1427T>G
ENST00000629016.2:c.227-4649T>G	ENSP00000486804.1:n.227-4649T>G
NM_000431.3:c.372-22T>G	NP_000422.1:n.372-22T>G
NM_001114185.2:c.372-22T>G	NP_001107657.1:n.372-22T>G
NM_001301182.1:c.371+1427T>G	NP_001288111.1:n.371+1427T>G
XM_011538372.1:c.372-22T>G	XP_011536674.1:n.372-22T>G
XM_017019313.2:c.371+1427T>G	XP_016874802.1:n.371+1427T>G
XM_017019314.1:c.372-22T>G	XP_016874803.1:n.372-22T>G
XM_024448982.1:c.372-22T>G	XP_024304750.1:n.372-22T>G
NM_000431.4:c.372-22T>G MANE Select	NP_000422.1:n.372-22T>G
NM_001114185.3:c.372-22T>G	NP_001107657.1:n.372-22T>G
NM_001301182.2:c.371+1427T>G	NP_001288111.1:n.371+1427T>G