Canonical Allele Identifier: CA2620818918

Gene: MVK

Linked Data

• gnomAD v4: 12-109596591-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109596591C>T , CM000674.2:g.109596591C>T	GRCh38
NC_000012.11:g.110034396C>T , CM000674.1:g.110034396C>T	GRCh37
NC_000012.10:g.108518779C>T	NCBI36
NG_007702.1:g.27897C>T , LRG_156:g.27897C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539696.6:c.*14C>T	ENSP00000439134.1:n.*14C>T
ENST00000546277.6:c.*14C>T	ENSP00000438153.2:n.*14C>T
ENST00000636529.2:n.844C>T
ENST00000697195.1:c.*969C>T	ENSP00000513181.1:n.*969C>T
ENST00000697196.1:c.*378C>T	ENSP00000513182.1:n.*378C>T
ENST00000697197.1:n.3234C>T
ENST00000697198.1:n.1589C>T
ENST00000228510.8:c.*14C>T MANE Select	ENSP00000228510.3:n.*14C>T
ENST00000636529.1:c.830C>T
ENST00000636996.1:c.1053C>T
ENST00000228510.7:c.*14C>T	ENSP00000228510.3:n.*14C>T
ENST00000392727.7:c.*14C>T	ENSP00000376487.3:n.*14C>T
ENST00000447878.6:c.*652C>T	ENSP00000415555.2:n.*652C>T
ENST00000539575.4:c.*14C>T	ENSP00000443551.2:n.*14C>T
ENST00000539696.5:c.*14C>T	ENSP00000439134.1:n.*14C>T
ENST00000540353.1:n.3438C>T
ENST00000625889.2:c.*14C>T	ENSP00000486846.1:n.*14C>T
ENST00000629016.2:c.*652C>T	ENSP00000486804.1:n.*652C>T
NM_000431.3:c.*14C>T	NP_000422.1:n.*14C>T
NM_001114185.2:c.*14C>T	NP_001107657.1:n.*14C>T
NM_001301182.1:c.*14C>T	NP_001288111.1:n.*14C>T
XM_011538372.1:c.*14C>T	XP_011536674.1:n.*14C>T
XM_017019313.2:c.*14C>T	XP_016874802.1:n.*14C>T
XM_017019314.1:c.*14C>T	XP_016874803.1:n.*14C>T
NM_000431.4:c.*14C>T MANE Select	NP_000422.1:n.*14C>T
NM_001114185.3:c.*14C>T	NP_001107657.1:n.*14C>T
NM_001301182.2:c.*14C>T	NP_001288111.1:n.*14C>T