Canonical Allele Identifier: CA353076962

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327143T>A (hg19) ; chr3:g.52293127T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293127T>A , CM000665.2:g.52293127T>A	GRCh38
NC_000003.11:g.52327143T>A , CM000665.1:g.52327143T>A	GRCh37
NC_000003.10:g.52302183T>A	NCBI36
NG_023246.1:g.10308T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000436784.7:c.*1T>A MANE Select	ENSP00000389175.2:n.*1T>A
ENST00000436784.6:c.*1T>A	ENSP00000389175.2:n.*1T>A
ENST00000461183.5:c.845T>A	ENSP00000417264.1:p.Met282Lys
ENST00000471180.5:c.716T>A	ENSP00000417526.1:p.Met239Lys
ENST00000473032.5:c.611T>A	ENSP00000418951.1:p.Met204Lys
ENST00000486393.5:c.*936T>A	ENSP00000419868.1:n.*936T>A
ENST00000489173.1:n.1867T>A
NM_145262.3:c.*1T>A	NP_660305.2:n.*1T>A
NR_026699.1:n.1671T>A
NR_026700.1:n.777T>A
NR_026701.1:n.1669T>A
NR_026702.1:n.707T>A
XM_005264878.2:c.*692T>A	XP_005264935.1:n.*692T>A
XR_245095.2:n.2824T>A
XM_017005730.1:c.*1T>A	XP_016861219.1:n.*1T>A
XM_024453351.1:c.*1T>A	XP_024309119.1:n.*1T>A
XM_024453352.1:c.*692T>A	XP_024309120.1:n.*692T>A
XR_001740022.2:n.3475T>A
XR_001740023.2:n.2999T>A
XR_245095.4:n.2825T>A
NM_145262.4:c.*1T>A MANE Select	NP_660305.2:n.*1T>A
NR_026699.2:n.1663T>A
NR_026700.2:n.769T>A
NR_026701.2:n.1661T>A
NR_026702.2:n.699T>A
NM_001144951.2:c.*692T>A	NP_001138423.1:n.*692T>A