Canonical Allele Identifier: CA2573332623

Gene: MVK

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109576029_109576031del , CM000674.2:g.109576029_109576031del	GRCh38
NC_000012.11:g.110013834_110013836del , CM000674.1:g.110013834_110013836del	GRCh37
NC_000012.10:g.108498217_108498219del	NCBI36
NG_007096.1:g.2467_2469del
NG_007702.1:g.7335_7337del , LRG_156:g.7335_7337del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539696.6:c.-92+2156_-92+2158del	ENSP00000439134.1:n.-92+2156_-92+2158del
ENST00000546277.6:c.110_112del	ENSP00000438153.2:p.Thr37_Phe38delinsIle
ENST00000636529.2:n.78+1129_78+1131del
ENST00000697195.1:c.110_112del	ENSP00000513181.1:p.Thr37_Phe38delinsIle
ENST00000697196.1:c.110_112del	ENSP00000513182.1:p.Thr37_Phe38delinsIle
ENST00000228510.8:c.110_112del MANE Select	ENSP00000228510.3:p.Thr37_Phe38delinsIle
ENST00000636529.1:c.64+1129_64+1131del
ENST00000636996.1:c.103_105del
ENST00000639206.1:c.110_112del	ENSP00000492778.1:p.Thr37_Phe38delinsIle
ENST00000228510.7:c.110_112del	ENSP00000228510.3:p.Thr37_Phe38delinsIle
ENST00000392727.7:c.110_112del	ENSP00000376487.3:p.Thr37_Phe38delinsIle
ENST00000447878.6:c.110_112del	ENSP00000415555.2:p.Thr37_Phe38delinsIle
ENST00000535044.1:n.355_357del
ENST00000537237.5:c.110_112del	ENSP00000445382.1:p.Thr37_Phe38delinsIle
ENST00000539335.5:c.110_112del	ENSP00000440379.1:p.Thr37_Phe38delinsIle
ENST00000539575.4:c.110_112del	ENSP00000443551.2:p.Thr37_Phe38delinsIle
ENST00000539696.5:c.-92+2156_-92+2158del	ENSP00000439134.1:n.-92+2156_-92+2158del
ENST00000545774.5:c.110_112del	ENSP00000443978.1:p.Thr37_Phe38delinsIle
ENST00000546277.5:c.110_112del	ENSP00000438153.1:p.Thr37_Phe38delinsIle
ENST00000625889.2:c.110_112del	ENSP00000486846.1:p.Thr37_Phe38delinsIle
ENST00000629016.2:c.110_112del	ENSP00000486804.1:p.Thr37_Phe38delinsIle
NM_000431.3:c.110_112del	NP_000422.1:p.Thr37_Phe38delinsIle
NM_001114185.2:c.110_112del	NP_001107657.1:p.Thr37_Phe38delinsIle
NM_001301182.1:c.110_112del	NP_001288111.1:p.Thr37_Phe38delinsIle
XM_011538372.1:c.110_112del	XP_011536674.1:p.Thr37_Phe38delinsIle
XM_017019313.2:c.110_112del	XP_016874802.1:p.Thr37_Phe38delinsIle
XM_017019314.1:c.110_112del	XP_016874803.1:p.Thr37_Phe38delinsIle
XM_024448982.1:c.110_112del	XP_024304750.1:p.Thr37_Phe38delinsIle
NM_000431.4:c.110_112del MANE Select	NP_000422.1:p.Thr37_Phe38delinsIle
NM_001114185.3:c.110_112del	NP_001107657.1:p.Thr37_Phe38delinsIle
NM_001301182.2:c.110_112del	NP_001288111.1:p.Thr37_Phe38delinsIle