Canonical Allele Identifier: CA2797414488

Gene: MVK

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109595353_109595354insGT , CM000674.2:g.109595353_109595354insGT	GRCh38
NC_000012.11:g.110033158_110033159insGT , CM000674.1:g.110033158_110033159insGT	GRCh37
NC_000012.10:g.108517541_108517542insGT	NCBI36
NG_007702.1:g.26659_26660insGT , LRG_156:g.26659_26660insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539696.6:c.196+172_196+173insGT	ENSP00000439134.1:n.196+172_196+173insGT
ENST00000546277.6:c.1039+172_1039+173insGT	ENSP00000438153.2:n.1039+172_1039+173insGT
ENST00000636529.2:n.678+172_678+173insGT
ENST00000697195.1:c.*803+172_*803+173insGT	ENSP00000513181.1:n.*803+172_*803+173insGT
ENST00000697196.1:c.*212+172_*212+173insGT	ENSP00000513182.1:n.*212+172_*212+173insGT
ENST00000697197.1:n.3068+172_3068+173insGT
ENST00000697198.1:n.1423+172_1423+173insGT
ENST00000228510.8:c.1039+172_1039+173insGT MANE Select	ENSP00000228510.3:n.1039+172_1039+173insGT
ENST00000636529.1:c.664+172_664+173insGT
ENST00000636996.1:c.887+172_887+173insGT
ENST00000228510.7:c.1039+172_1039+173insGT	ENSP00000228510.3:n.1039+172_1039+173insGT
ENST00000392727.7:c.883+172_883+173insGT	ENSP00000376487.3:n.883+172_883+173insGT
ENST00000447878.6:c.*486+172_*486+173insGT	ENSP00000415555.2:n.*486+172_*486+173insGT
ENST00000537237.5:c.*712+172_*712+173insGT	ENSP00000445382.1:n.*712+172_*712+173insGT
ENST00000539575.4:c.1039+172_1039+173insGT	ENSP00000443551.2:n.1039+172_1039+173insGT
ENST00000539696.5:c.196+172_196+173insGT	ENSP00000439134.1:n.196+172_196+173insGT
ENST00000540353.1:n.3272+172_3272+173insGT
ENST00000625889.2:c.883+172_883+173insGT	ENSP00000486846.1:n.883+172_883+173insGT
ENST00000629016.2:c.*486+172_*486+173insGT	ENSP00000486804.1:n.*486+172_*486+173insGT
NM_000431.3:c.1039+172_1039+173insGT	NP_000422.1:n.1039+172_1039+173insGT
NM_001114185.2:c.1039+172_1039+173insGT	NP_001107657.1:n.1039+172_1039+173insGT
NM_001301182.1:c.883+172_883+173insGT	NP_001288111.1:n.883+172_883+173insGT
XM_011538372.1:c.1039+172_1039+173insGT	XP_011536674.1:n.1039+172_1039+173insGT
XM_017019313.2:c.883+172_883+173insGT	XP_016874802.1:n.883+172_883+173insGT
XM_017019314.1:c.1039+172_1039+173insGT	XP_016874803.1:n.1039+172_1039+173insGT
NM_000431.4:c.1039+172_1039+173insGT MANE Select	NP_000422.1:n.1039+172_1039+173insGT
NM_001114185.3:c.1039+172_1039+173insGT	NP_001107657.1:n.1039+172_1039+173insGT
NM_001301182.2:c.883+172_883+173insGT	NP_001288111.1:n.883+172_883+173insGT