Canonical Allele Identifier: CA353076966

Gene: GLYCTK

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*1T>C MANE Select	ENSP00000389175.2:n.*1T>C
ENST00000436784.6:c.*1T>C	ENSP00000389175.2:n.*1T>C
ENST00000461183.5:c.845T>C	ENSP00000417264.1:p.Met282Thr
ENST00000471180.5:c.716T>C	ENSP00000417526.1:p.Met239Thr
ENST00000473032.5:c.611T>C	ENSP00000418951.1:p.Met204Thr
ENST00000486393.5:c.*936T>C	ENSP00000419868.1:n.*936T>C
ENST00000489173.1:n.1867T>C
NM_145262.3:c.*1T>C	NP_660305.2:n.*1T>C
NR_026699.1:n.1671T>C
NR_026700.1:n.777T>C
NR_026701.1:n.1669T>C
NR_026702.1:n.707T>C
XM_005264878.2:c.*692T>C	XP_005264935.1:n.*692T>C
XR_245095.2:n.2824T>C
XM_017005730.1:c.*1T>C	XP_016861219.1:n.*1T>C
XM_024453351.1:c.*1T>C	XP_024309119.1:n.*1T>C
XM_024453352.1:c.*692T>C	XP_024309120.1:n.*692T>C
XR_001740022.2:n.3475T>C
XR_001740023.2:n.2999T>C
XR_245095.4:n.2825T>C
NM_145262.4:c.*1T>C MANE Select	NP_660305.2:n.*1T>C
NR_026699.2:n.1663T>C
NR_026700.2:n.769T>C
NR_026701.2:n.1661T>C
NR_026702.2:n.699T>C
NM_001144951.2:c.*692T>C	NP_001138423.1:n.*692T>C