Canonical Allele Identifier: CA353075321

Gene: GLYCTK

Linked Data

• gnomAD v4: 3-52292704-C-T
• MyVariant Identifiers: chr3:g.52326720C>T (hg19) ; chr3:g.52292704C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292704C>T , CM000665.2:g.52292704C>T	GRCh38
NC_000003.11:g.52326720C>T , CM000665.1:g.52326720C>T	GRCh37
NC_000003.10:g.52301760C>T	NCBI36
NG_023246.1:g.9885C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1150C>T MANE Select	ENSP00000389175.2:p.Pro384Ser
ENST00000305690.12:c.*269C>T	ENSP00000301965.9:n.*269C>T
ENST00000436784.6:c.1150C>T	ENSP00000389175.2:p.Pro384Ser
ENST00000461183.5:c.763+135C>T	ENSP00000417264.1:n.763+135C>T
ENST00000471180.5:c.634+135C>T	ENSP00000417526.1:n.634+135C>T
ENST00000473032.5:c.530-342C>T	ENSP00000418951.1:n.530-342C>T
ENST00000477382.1:c.*269C>T	ENSP00000419008.1:n.*269C>T
ENST00000486393.5:c.*513C>T	ENSP00000419868.1:n.*513C>T
ENST00000489173.1:n.1444C>T
NM_001144951.1:c.*269C>T	NP_001138423.1:n.*269C>T
NM_145262.3:c.1150C>T	NP_660305.2:p.Pro384Ser
NR_026699.1:n.1248C>T
NR_026700.1:n.695+135C>T
NR_026701.1:n.1246C>T
NR_026702.1:n.626-342C>T
XM_005264878.2:c.*269C>T	XP_005264935.1:n.*269C>T
XR_245095.2:n.2742+135C>T
XM_017005730.1:c.769C>T	XP_016861219.1:p.Pro257Ser
XM_024453351.1:c.1150C>T	XP_024309119.1:p.Pro384Ser
XM_024453352.1:c.*269C>T	XP_024309120.1:n.*269C>T
XR_001740022.2:n.3052C>T
XR_001740023.2:n.2917+135C>T
XR_245095.4:n.2743+135C>T
NM_145262.4:c.1150C>T MANE Select	NP_660305.2:p.Pro384Ser
NR_026699.2:n.1240C>T
NR_026700.2:n.687+135C>T
NR_026701.2:n.1238C>T
NR_026702.2:n.618-342C>T
NM_001144951.2:c.*269C>T	NP_001138423.1:n.*269C>T