Canonical Allele Identifier: CA353076979

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327145G>T (hg19) ; chr3:g.52293129G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293129G>T , CM000665.2:g.52293129G>T	GRCh38
NC_000003.11:g.52327145G>T , CM000665.1:g.52327145G>T	GRCh37
NC_000003.10:g.52302185G>T	NCBI36
NG_023246.1:g.10310G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000436784.7:c.*3G>T MANE Select	ENSP00000389175.2:n.*3G>T
ENST00000436784.6:c.*3G>T	ENSP00000389175.2:n.*3G>T
ENST00000461183.5:c.847G>T	ENSP00000417264.1:p.Ala283Ser
ENST00000471180.5:c.718G>T	ENSP00000417526.1:p.Ala240Ser
ENST00000473032.5:c.613G>T	ENSP00000418951.1:p.Ala205Ser
ENST00000486393.5:c.*938G>T	ENSP00000419868.1:n.*938G>T
ENST00000489173.1:n.1869G>T
NM_145262.3:c.*3G>T	NP_660305.2:n.*3G>T
NR_026699.1:n.1673G>T
NR_026700.1:n.779G>T
NR_026701.1:n.1671G>T
NR_026702.1:n.709G>T
XM_005264878.2:c.*694G>T	XP_005264935.1:n.*694G>T
XR_245095.2:n.2826G>T
XM_017005730.1:c.*3G>T	XP_016861219.1:n.*3G>T
XM_024453351.1:c.*3G>T	XP_024309119.1:n.*3G>T
XM_024453352.1:c.*694G>T	XP_024309120.1:n.*694G>T
XR_001740022.2:n.3477G>T
XR_001740023.2:n.3001G>T
XR_245095.4:n.2827G>T
NM_145262.4:c.*3G>T MANE Select	NP_660305.2:n.*3G>T
NR_026699.2:n.1665G>T
NR_026700.2:n.771G>T
NR_026701.2:n.1663G>T
NR_026702.2:n.701G>T
NM_001144951.2:c.*694G>T	NP_001138423.1:n.*694G>T