Canonical Allele Identifier: CA481714711
Gene: MVK HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.110028579G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.109590774G>T , CM000674.2:g.109590774G>T GRCh38
NC_000012.11:g.110028579G>T , CM000674.1:g.110028579G>T GRCh37
NC_000012.10:g.108512962G>T NCBI36
NG_007702.1:g.22080G>T , LRG_156:g.22080G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000539696.6:c.-91-72G>T ENSP00000439134.1:n.-91-72G>T
ENST00000546277.6:c.681G>T ENSP00000438153.2:p.Ser227=
ENST00000636529.2:n.320G>T
ENST00000697195.1:c.*445G>T ENSP00000513181.1:n.*445G>T
ENST00000697196.1:c.769G>T ENSP00000513182.1:p.Ala257Ser
ENST00000697197.1:n.2331G>T
ENST00000228510.8:c.681G>T MANE Select ENSP00000228510.3:p.Ser227=
ENST00000636529.1:c.306G>T
ENST00000636996.1:c.529G>T
ENST00000228510.7:c.681G>T ENSP00000228510.3:p.Ser227=
ENST00000392727.7:c.525G>T ENSP00000376487.3:p.Ser175=
ENST00000447878.6:c.*128G>T ENSP00000415555.2:n.*128G>T
ENST00000537237.5:c.*442-467G>T ENSP00000445382.1:n.*442-467G>T
ENST00000539575.4:c.681G>T ENSP00000443551.2:p.Ser227=
ENST00000539696.5:c.-91-72G>T ENSP00000439134.1:n.-91-72G>T
ENST00000540353.1:n.2914G>T
ENST00000625889.2:c.525G>T ENSP00000486846.1:p.Ser175=
ENST00000629016.2:c.*128G>T ENSP00000486804.1:n.*128G>T
NM_000431.3:c.681G>T NP_000422.1:p.Ser227=
NM_001114185.2:c.681G>T NP_001107657.1:p.Ser227=
NM_001301182.1:c.525G>T NP_001288111.1:p.Ser175=
XM_011538372.1:c.681G>T XP_011536674.1:p.Ser227=
XM_017019313.2:c.525G>T XP_016874802.1:p.Ser175=
XM_017019314.1:c.681G>T XP_016874803.1:p.Ser227=
XM_024448982.1:c.681G>T XP_024304750.1:p.Ser227=
NM_000431.4:c.681G>T MANE Select NP_000422.1:p.Ser227=
NM_001114185.3:c.681G>T NP_001107657.1:p.Ser227=
NM_001301182.2:c.525G>T NP_001288111.1:p.Ser175=