Canonical Allele Identifier: CA2062473016

Gene: MVK

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109596286_109596287delinsTG , CM000674.2:g.109596286_109596287delinsTG	GRCh38
NC_000012.11:g.110034091_110034092delinsTG , CM000674.1:g.110034091_110034092delinsTG	GRCh37
NC_000012.10:g.108518474_108518475delinsTG	NCBI36
NG_007702.1:g.27592_27593delinsTG , LRG_156:g.27592_27593delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539696.6:c.197-140_197-139delinsTG	ENSP00000439134.1:n.197-140_197-139delinsTG
ENST00000546277.6:c.1040-140_1040-139delinsTG	ENSP00000438153.2:n.1040-140_1040-139delinsTG
ENST00000636529.2:n.679-140_679-139delinsTG
ENST00000697195.1:c.*804-140_*804-139delinsTG	ENSP00000513181.1:n.*804-140_*804-139delinsTG
ENST00000697196.1:c.*213-140_*213-139delinsTG	ENSP00000513182.1:n.*213-140_*213-139delinsTG
ENST00000697197.1:n.3069-140_3069-139delinsTG
ENST00000697198.1:n.1424-140_1424-139delinsTG
ENST00000228510.8:c.1040-140_1040-139delinsTG MANE Select	ENSP00000228510.3:n.1040-140_1040-139delinsTG
ENST00000636529.1:c.665-140_665-139delinsTG
ENST00000636996.1:c.888-140_888-139delinsTG
ENST00000228510.7:c.1040-140_1040-139delinsTG	ENSP00000228510.3:n.1040-140_1040-139delinsTG
ENST00000392727.7:c.884-140_884-139delinsTG	ENSP00000376487.3:n.884-140_884-139delinsTG
ENST00000447878.6:c.*487-140_*487-139delinsTG	ENSP00000415555.2:n.*487-140_*487-139delinsTG
ENST00000537237.5:c.*713-140_*713-139delinsTG	ENSP00000445382.1:n.*713-140_*713-139delinsTG
ENST00000539575.4:c.1040-140_1040-139delinsTG	ENSP00000443551.2:n.1040-140_1040-139delinsTG
ENST00000539696.5:c.197-140_197-139delinsTG	ENSP00000439134.1:n.197-140_197-139delinsTG
ENST00000540353.1:n.3273-140_3273-139delinsTG
ENST00000625889.2:c.884-140_884-139delinsTG	ENSP00000486846.1:n.884-140_884-139delinsTG
ENST00000629016.2:c.*487-140_*487-139delinsTG	ENSP00000486804.1:n.*487-140_*487-139delinsTG
NM_000431.3:c.1040-140_1040-139delinsTG	NP_000422.1:n.1040-140_1040-139delinsTG
NM_001114185.2:c.1040-140_1040-139delinsTG	NP_001107657.1:n.1040-140_1040-139delinsTG
NM_001301182.1:c.884-140_884-139delinsTG	NP_001288111.1:n.884-140_884-139delinsTG
XM_011538372.1:c.1040-140_1040-139delinsTG	XP_011536674.1:n.1040-140_1040-139delinsTG
XM_017019313.2:c.884-140_884-139delinsTG	XP_016874802.1:n.884-140_884-139delinsTG
XM_017019314.1:c.1040-140_1040-139delinsTG	XP_016874803.1:n.1040-140_1040-139delinsTG
NM_000431.4:c.1040-140_1040-139delinsTG MANE Select	NP_000422.1:n.1040-140_1040-139delinsTG
NM_001114185.3:c.1040-140_1040-139delinsTG	NP_001107657.1:n.1040-140_1040-139delinsTG
NM_001301182.2:c.884-140_884-139delinsTG	NP_001288111.1:n.884-140_884-139delinsTG