Canonical Allele Identifier: CA353074645

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52326595A>C (hg19) ; chr3:g.52292579A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292579A>C , CM000665.2:g.52292579A>C	GRCh38
NC_000003.11:g.52326595A>C , CM000665.1:g.52326595A>C	GRCh37
NC_000003.10:g.52301635A>C	NCBI36
NG_023246.1:g.9760A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1025A>C MANE Select	ENSP00000389175.2:p.Lys342Thr
ENST00000305690.12:c.*144A>C	ENSP00000301965.9:n.*144A>C
ENST00000436784.6:c.1025A>C	ENSP00000389175.2:p.Lys342Thr
ENST00000461183.5:c.763+10A>C	ENSP00000417264.1:n.763+10A>C
ENST00000471180.5:c.634+10A>C	ENSP00000417526.1:n.634+10A>C
ENST00000473032.5:c.530-467A>C	ENSP00000418951.1:n.530-467A>C
ENST00000477382.1:c.*144A>C	ENSP00000419008.1:n.*144A>C
ENST00000486393.5:c.*388A>C	ENSP00000419868.1:n.*388A>C
ENST00000489173.1:n.1319A>C
NM_001144951.1:c.*144A>C	NP_001138423.1:n.*144A>C
NM_145262.3:c.1025A>C	NP_660305.2:p.Lys342Thr
NR_026699.1:n.1123A>C
NR_026700.1:n.695+10A>C
NR_026701.1:n.1121A>C
NR_026702.1:n.626-467A>C
XM_005264878.2:c.*144A>C	XP_005264935.1:n.*144A>C
XR_245095.2:n.2742+10A>C
XM_017005730.1:c.644A>C	XP_016861219.1:p.Lys215Thr
XM_024453351.1:c.1025A>C	XP_024309119.1:p.Lys342Thr
XM_024453352.1:c.*144A>C	XP_024309120.1:n.*144A>C
XR_001740022.2:n.2927A>C
XR_001740023.2:n.2917+10A>C
XR_245095.4:n.2743+10A>C
NM_145262.4:c.1025A>C MANE Select	NP_660305.2:p.Lys342Thr
NR_026699.2:n.1115A>C
NR_026700.2:n.687+10A>C
NR_026701.2:n.1113A>C
NR_026702.2:n.618-467A>C
NM_001144951.2:c.*144A>C	NP_001138423.1:n.*144A>C