Canonical Allele Identifier: CA2620812785

Gene: MVK

Linked Data

• gnomAD v4: 12-109574802-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109574806del , CM000674.2:g.109574806del	GRCh38
NC_000012.11:g.110012611del , CM000674.1:g.110012611del	GRCh37
NC_000012.10:g.108496994del	NCBI36
NG_007096.1:g.3695del
NG_007702.1:g.6112del , LRG_156:g.6112del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539696.6:c.-92+933del	ENSP00000439134.1:n.-92+933del
ENST00000546277.6:c.-14-3del	ENSP00000438153.2:n.-14-3del
ENST00000697195.1:c.-17del	ENSP00000513181.1:n.-17del
ENST00000228510.8:c.-14-3del MANE Select	ENSP00000228510.3:n.-14-3del
ENST00000228510.7:c.-14-3del	ENSP00000228510.3:n.-14-3del
ENST00000392727.7:c.-14-3del	ENSP00000376487.3:n.-14-3del
ENST00000447878.6:c.-14-3del	ENSP00000415555.2:n.-14-3del
ENST00000535044.1:n.232-3del
ENST00000537237.5:c.-14-3del	ENSP00000445382.1:n.-14-3del
ENST00000539335.5:c.-5-12del	ENSP00000440379.1:n.-5-12del
ENST00000539696.5:c.-92+933del	ENSP00000439134.1:n.-92+933del
ENST00000545774.5:c.-14-3del	ENSP00000443978.1:n.-14-3del
ENST00000546277.5:c.-14-3del	ENSP00000438153.1:n.-14-3del
NM_000431.3:c.-14-3del	NP_000422.1:n.-14-3del
NM_001114185.2:c.-5-12del	NP_001107657.1:n.-5-12del
NM_001301182.1:c.-14-3del	NP_001288111.1:n.-14-3del
XM_011538372.1:c.-14-3del	XP_011536674.1:n.-14-3del
XM_017019313.2:c.-14-3del	XP_016874802.1:n.-14-3del
XM_017019314.1:c.-14-3del	XP_016874803.1:n.-14-3del
XM_024448982.1:c.-14-3del	XP_024304750.1:n.-14-3del
NM_000431.4:c.-14-3del MANE Select	NP_000422.1:n.-14-3del
NM_001114185.3:c.-5-12del	NP_001107657.1:n.-5-12del
NM_001301182.2:c.-14-3del	NP_001288111.1:n.-14-3del