Canonical Allele Identifier: CA2062460067

Gene: MVK

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109574787_109574795delinsTCTCATTGG , CM000674.2:g.109574787_109574795delinsTCTCATTGG	GRCh38
NC_000012.11:g.110012592_110012600delinsTCTCATTGG , CM000674.1:g.110012592_110012600delinsTCTCATTGG	GRCh37
NC_000012.10:g.108496975_108496983delinsTCTCATTGG	NCBI36
NG_007096.1:g.3703_3711delinsCCAATGAGA
NG_007702.1:g.6093_6101delinsTCTCATTGG , LRG_156:g.6093_6101delinsTCTCATTGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000539696.6:c.-92+914_-92+922delinsTCTCATTGG	ENSP00000439134.1:n.-92+914_-92+922delinsTCTCATTGG
ENST00000546277.6:c.-14-22_-14-14delinsTCTCATTGG	ENSP00000438153.2:n.-14-22_-14-14delinsTCTCATTGG
ENST00000697195.1:c.-36_-28delinsTCTCATTGG	ENSP00000513181.1:n.-36_-28delinsTCTCATTGG
ENST00000228510.8:c.-14-22_-14-14delinsTCTCATTGG MANE Select	ENSP00000228510.3:n.-14-22_-14-14delinsTCTCATTGG
ENST00000228510.7:c.-14-22_-14-14delinsTCTCATTGG	ENSP00000228510.3:n.-14-22_-14-14delinsTCTCATTGG
ENST00000392727.7:c.-14-22_-14-14delinsTCTCATTGG	ENSP00000376487.3:n.-14-22_-14-14delinsTCTCATTGG
ENST00000447878.6:c.-14-22_-14-14delinsTCTCATTGG	ENSP00000415555.2:n.-14-22_-14-14delinsTCTCATTGG
ENST00000535044.1:n.232-22_232-14delinsTCTCATTGG
ENST00000537237.5:c.-14-22_-14-14delinsTCTCATTGG	ENSP00000445382.1:n.-14-22_-14-14delinsTCTCATTGG
ENST00000539335.5:c.-5-31_-5-23delinsTCTCATTGG	ENSP00000440379.1:n.-5-31_-5-23delinsTCTCATTGG
ENST00000539696.5:c.-92+914_-92+922delinsTCTCATTGG	ENSP00000439134.1:n.-92+914_-92+922delinsTCTCATTGG
ENST00000545774.5:c.-14-22_-14-14delinsTCTCATTGG	ENSP00000443978.1:n.-14-22_-14-14delinsTCTCATTGG
ENST00000546277.5:c.-14-22_-14-14delinsTCTCATTGG	ENSP00000438153.1:n.-14-22_-14-14delinsTCTCATTGG
NM_000431.3:c.-14-22_-14-14delinsTCTCATTGG	NP_000422.1:n.-14-22_-14-14delinsTCTCATTGG
NM_001114185.2:c.-5-31_-5-23delinsTCTCATTGG	NP_001107657.1:n.-5-31_-5-23delinsTCTCATTGG
NM_001301182.1:c.-14-22_-14-14delinsTCTCATTGG	NP_001288111.1:n.-14-22_-14-14delinsTCTCATTGG
XM_011538372.1:c.-14-22_-14-14delinsTCTCATTGG	XP_011536674.1:n.-14-22_-14-14delinsTCTCATTGG
XM_017019313.2:c.-14-22_-14-14delinsTCTCATTGG	XP_016874802.1:n.-14-22_-14-14delinsTCTCATTGG
XM_017019314.1:c.-14-22_-14-14delinsTCTCATTGG	XP_016874803.1:n.-14-22_-14-14delinsTCTCATTGG
XM_024448982.1:c.-14-22_-14-14delinsTCTCATTGG	XP_024304750.1:n.-14-22_-14-14delinsTCTCATTGG
NM_000431.4:c.-14-22_-14-14delinsTCTCATTGG MANE Select	NP_000422.1:n.-14-22_-14-14delinsTCTCATTGG
NM_001114185.3:c.-5-31_-5-23delinsTCTCATTGG	NP_001107657.1:n.-5-31_-5-23delinsTCTCATTGG
NM_001301182.2:c.-14-22_-14-14delinsTCTCATTGG	NP_001288111.1:n.-14-22_-14-14delinsTCTCATTGG