Canonical Allele Identifier: CA2580085781

Gene: MVK

Linked Data

• ClinVar Variation Id: 2099425
• ClinVar RCV Id: RCV003021716

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109595188dup , CM000674.2:g.109595188dup	GRCh38
NC_000012.11:g.110032993dup , CM000674.1:g.110032993dup	GRCh37
NC_000012.10:g.108517376dup	NCBI36
NG_007702.1:g.26494dup , LRG_156:g.26494dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539696.6:c.196+7dup	ENSP00000439134.1:n.196+7dup
ENST00000546277.6:c.1039+7dup	ENSP00000438153.2:n.1039+7dup
ENST00000636529.2:n.678+7dup
ENST00000697195.1:c.*803+7dup	ENSP00000513181.1:n.*803+7dup
ENST00000697196.1:c.*212+7dup	ENSP00000513182.1:n.*212+7dup
ENST00000697197.1:n.3068+7dup
ENST00000697198.1:n.1423+7dup
ENST00000228510.8:c.1039+7dup MANE Select	ENSP00000228510.3:n.1039+7dup
ENST00000636529.1:c.664+7dup
ENST00000636996.1:c.887+7dup
ENST00000228510.7:c.1039+7dup	ENSP00000228510.3:n.1039+7dup
ENST00000392727.7:c.883+7dup	ENSP00000376487.3:n.883+7dup
ENST00000447878.6:c.*486+7dup	ENSP00000415555.2:n.*486+7dup
ENST00000537237.5:c.*712+7dup	ENSP00000445382.1:n.*712+7dup
ENST00000539575.4:c.1039+7dup	ENSP00000443551.2:n.1039+7dup
ENST00000539696.5:c.196+7dup	ENSP00000439134.1:n.196+7dup
ENST00000540353.1:n.3272+7dup
ENST00000625889.2:c.883+7dup	ENSP00000486846.1:n.883+7dup
ENST00000629016.2:c.*486+7dup	ENSP00000486804.1:n.*486+7dup
NM_000431.3:c.1039+7dup	NP_000422.1:n.1039+7dup
NM_001114185.2:c.1039+7dup	NP_001107657.1:n.1039+7dup
NM_001301182.1:c.883+7dup	NP_001288111.1:n.883+7dup
XM_011538372.1:c.1039+7dup	XP_011536674.1:n.1039+7dup
XM_017019313.2:c.883+7dup	XP_016874802.1:n.883+7dup
XM_017019314.1:c.1039+7dup	XP_016874803.1:n.1039+7dup
NM_000431.4:c.1039+7dup MANE Select	NP_000422.1:n.1039+7dup
NM_001114185.3:c.1039+7dup	NP_001107657.1:n.1039+7dup
NM_001301182.2:c.883+7dup	NP_001288111.1:n.883+7dup