Canonical Allele Identifier: CA433752046

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327147A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293131A>T , CM000665.2:g.52293131A>T	GRCh38
NC_000003.11:g.52327147A>T , CM000665.1:g.52327147A>T	GRCh37
NC_000003.10:g.52302187A>T	NCBI36
NG_023246.1:g.10312A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*5A>T MANE Select	ENSP00000389175.2:n.*5A>T
ENST00000436784.6:c.*5A>T	ENSP00000389175.2:n.*5A>T
ENST00000461183.5:c.849A>T	ENSP00000417264.1:p.Ala283=
ENST00000471180.5:c.720A>T	ENSP00000417526.1:p.Ala240=
ENST00000473032.5:c.615A>T	ENSP00000418951.1:p.Ala205=
ENST00000486393.5:c.*940A>T	ENSP00000419868.1:n.*940A>T
ENST00000489173.1:n.1871A>T
NM_145262.3:c.*5A>T	NP_660305.2:n.*5A>T
NR_026699.1:n.1675A>T
NR_026700.1:n.781A>T
NR_026701.1:n.1673A>T
NR_026702.1:n.711A>T
XM_005264878.2:c.*696A>T	XP_005264935.1:n.*696A>T
XR_245095.2:n.2828A>T
XM_017005730.1:c.*5A>T	XP_016861219.1:n.*5A>T
XM_024453351.1:c.*5A>T	XP_024309119.1:n.*5A>T
XM_024453352.1:c.*696A>T	XP_024309120.1:n.*696A>T
XR_001740022.2:n.3479A>T
XR_001740023.2:n.3003A>T
XR_245095.4:n.2829A>T
NM_145262.4:c.*5A>T MANE Select	NP_660305.2:n.*5A>T
NR_026699.2:n.1667A>T
NR_026700.2:n.773A>T
NR_026701.2:n.1665A>T
NR_026702.2:n.703A>T
NM_001144951.2:c.*696A>T	NP_001138423.1:n.*696A>T