Canonical Allele Identifier: CA2620818579

Gene: MVK

Linked Data

• gnomAD v4: 12-109591484-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109591484G>T , CM000674.2:g.109591484G>T	GRCh38
NC_000012.11:g.110029289G>T , CM000674.1:g.110029289G>T	GRCh37
NC_000012.10:g.108513672G>T	NCBI36
NG_007702.1:g.22790G>T , LRG_156:g.22790G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539696.6:c.42+127G>T	ENSP00000439134.1:n.42+127G>T
ENST00000546277.6:c.885+127G>T	ENSP00000438153.2:n.885+127G>T
ENST00000636529.2:n.524+127G>T
ENST00000697195.1:c.*649+127G>T	ENSP00000513181.1:n.*649+127G>T
ENST00000697196.1:c.*58+127G>T	ENSP00000513182.1:n.*58+127G>T
ENST00000697197.1:n.2914+127G>T
ENST00000228510.8:c.885+127G>T MANE Select	ENSP00000228510.3:n.885+127G>T
ENST00000636529.1:c.510+127G>T
ENST00000636996.1:c.733+127G>T
ENST00000228510.7:c.885+127G>T	ENSP00000228510.3:n.885+127G>T
ENST00000392727.7:c.729+127G>T	ENSP00000376487.3:n.729+127G>T
ENST00000447878.6:c.*332+127G>T	ENSP00000415555.2:n.*332+127G>T
ENST00000537237.5:c.*558+127G>T	ENSP00000445382.1:n.*558+127G>T
ENST00000539575.4:c.885+127G>T	ENSP00000443551.2:n.885+127G>T
ENST00000539696.5:c.42+127G>T	ENSP00000439134.1:n.42+127G>T
ENST00000540353.1:n.3118+127G>T
ENST00000625889.2:c.729+127G>T	ENSP00000486846.1:n.729+127G>T
ENST00000629016.2:c.*332+127G>T	ENSP00000486804.1:n.*332+127G>T
NM_000431.3:c.885+127G>T	NP_000422.1:n.885+127G>T
NM_001114185.2:c.885+127G>T	NP_001107657.1:n.885+127G>T
NM_001301182.1:c.729+127G>T	NP_001288111.1:n.729+127G>T
XM_011538372.1:c.885+127G>T	XP_011536674.1:n.885+127G>T
XM_017019313.2:c.729+127G>T	XP_016874802.1:n.729+127G>T
XM_017019314.1:c.885+127G>T	XP_016874803.1:n.885+127G>T
XM_024448982.1:c.1012G>T	XP_024304750.1:p.Ala338Ser
NM_000431.4:c.885+127G>T MANE Select	NP_000422.1:n.885+127G>T
NM_001114185.3:c.885+127G>T	NP_001107657.1:n.885+127G>T
NM_001301182.2:c.729+127G>T	NP_001288111.1:n.729+127G>T