Canonical Allele Identifier: CA2740092592

Gene: MVK

Linked Data

• ClinVar Variation Id: 2943228
• ClinVar RCV Id: RCV003800346

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109574868_109574871del , CM000674.2:g.109574868_109574871del	GRCh38
NC_000012.11:g.110012673_110012676del , CM000674.1:g.110012673_110012676del	GRCh37
NC_000012.10:g.108497056_108497059del	NCBI36
NG_007096.1:g.3629_3632del
NG_007702.1:g.6174_6177del , LRG_156:g.6174_6177del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539696.6:c.-92+995_-92+998del	ENSP00000439134.1:n.-92+995_-92+998del
ENST00000546277.6:c.46_49del	ENSP00000438153.2:p.Leu16MetfsTer11
ENST00000636529.2:n.46_49del
ENST00000697195.1:c.46_49del	ENSP00000513181.1:p.Leu16MetfsTer11
ENST00000697196.1:c.46_49del	ENSP00000513182.1:p.Leu16MetfsTer11
ENST00000228510.8:c.46_49del MANE Select	ENSP00000228510.3:p.Leu16MetfsTer11
ENST00000636529.1:c.32_35del
ENST00000636996.1:c.39_42del
ENST00000639206.1:c.46_49del	ENSP00000492778.1:p.Leu16MetfsTer11
ENST00000228510.7:c.46_49del	ENSP00000228510.3:p.Leu16MetfsTer11
ENST00000392727.7:c.46_49del	ENSP00000376487.3:p.Leu16MetfsTer11
ENST00000447878.6:c.46_49del	ENSP00000415555.2:p.Leu16MetfsTer11
ENST00000535044.1:n.291_294del
ENST00000537237.5:c.46_49del	ENSP00000445382.1:p.Leu16MetfsTer11
ENST00000539335.5:c.46_49del	ENSP00000440379.1:p.Leu16MetfsTer11
ENST00000539575.4:c.46_49del	ENSP00000443551.2:p.Leu16MetfsTer11
ENST00000539696.5:c.-92+995_-92+998del	ENSP00000439134.1:n.-92+995_-92+998del
ENST00000545774.5:c.46_49del	ENSP00000443978.1:p.Leu16MetfsTer11
ENST00000546277.5:c.46_49del	ENSP00000438153.1:p.Leu16MetfsTer11
ENST00000625889.2:c.46_49del	ENSP00000486846.1:p.Leu16MetfsTer11
ENST00000629016.2:c.46_49del	ENSP00000486804.1:p.Leu16MetfsTer11
NM_000431.3:c.46_49del	NP_000422.1:p.Leu16MetfsTer11
NM_001114185.2:c.46_49del	NP_001107657.1:p.Leu16MetfsTer11
NM_001301182.1:c.46_49del	NP_001288111.1:p.Leu16MetfsTer11
XM_011538372.1:c.46_49del	XP_011536674.1:p.Leu16MetfsTer11
XM_017019313.2:c.46_49del	XP_016874802.1:p.Leu16MetfsTer11
XM_017019314.1:c.46_49del	XP_016874803.1:p.Leu16MetfsTer11
XM_024448982.1:c.46_49del	XP_024304750.1:p.Leu16MetfsTer11
NM_000431.4:c.46_49del MANE Select	NP_000422.1:p.Leu16MetfsTer11
NM_001114185.3:c.46_49del	NP_001107657.1:p.Leu16MetfsTer11
NM_001301182.2:c.46_49del	NP_001288111.1:p.Leu16MetfsTer11