Canonical Allele Identifier: CA2620818846

Gene: MVK

Linked Data

• gnomAD v4: 12-109596326-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109596328del , CM000674.2:g.109596328del	GRCh38
NC_000012.11:g.110034133del , CM000674.1:g.110034133del	GRCh37
NC_000012.10:g.108518516del	NCBI36
NG_007702.1:g.27634del , LRG_156:g.27634del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539696.6:c.197-98del	ENSP00000439134.1:n.197-98del
ENST00000546277.6:c.1040-98del	ENSP00000438153.2:n.1040-98del
ENST00000636529.2:n.679-98del
ENST00000697195.1:c.*804-98del	ENSP00000513181.1:n.*804-98del
ENST00000697196.1:c.*213-98del	ENSP00000513182.1:n.*213-98del
ENST00000697197.1:n.3069-98del
ENST00000697198.1:n.1424-98del
ENST00000228510.8:c.1040-98del MANE Select	ENSP00000228510.3:n.1040-98del
ENST00000636529.1:c.665-98del
ENST00000636996.1:c.888-98del
ENST00000228510.7:c.1040-98del	ENSP00000228510.3:n.1040-98del
ENST00000392727.7:c.884-98del	ENSP00000376487.3:n.884-98del
ENST00000447878.6:c.*487-98del	ENSP00000415555.2:n.*487-98del
ENST00000537237.5:c.*713-98del	ENSP00000445382.1:n.*713-98del
ENST00000539575.4:c.1040-98del	ENSP00000443551.2:n.1040-98del
ENST00000539696.5:c.197-98del	ENSP00000439134.1:n.197-98del
ENST00000540353.1:n.3273-98del
ENST00000625889.2:c.884-98del	ENSP00000486846.1:n.884-98del
ENST00000629016.2:c.*487-98del	ENSP00000486804.1:n.*487-98del
NM_000431.3:c.1040-98del	NP_000422.1:n.1040-98del
NM_001114185.2:c.1040-98del	NP_001107657.1:n.1040-98del
NM_001301182.1:c.884-98del	NP_001288111.1:n.884-98del
XM_011538372.1:c.1040-98del	XP_011536674.1:n.1040-98del
XM_017019313.2:c.884-98del	XP_016874802.1:n.884-98del
XM_017019314.1:c.1040-98del	XP_016874803.1:n.1040-98del
NM_000431.4:c.1040-98del MANE Select	NP_000422.1:n.1040-98del
NM_001114185.3:c.1040-98del	NP_001107657.1:n.1040-98del
NM_001301182.2:c.884-98del	NP_001288111.1:n.884-98del