Canonical Allele Identifier: CA433883030

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52326695T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292679T>C , CM000665.2:g.52292679T>C	GRCh38
NC_000003.11:g.52326695T>C , CM000665.1:g.52326695T>C	GRCh37
NC_000003.10:g.52301735T>C	NCBI36
NG_023246.1:g.9860T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1125T>C MANE Select	ENSP00000389175.2:p.His375=
ENST00000305690.12:c.*244T>C	ENSP00000301965.9:n.*244T>C
ENST00000436784.6:c.1125T>C	ENSP00000389175.2:p.His375=
ENST00000461183.5:c.763+110T>C	ENSP00000417264.1:n.763+110T>C
ENST00000471180.5:c.634+110T>C	ENSP00000417526.1:n.634+110T>C
ENST00000473032.5:c.530-367T>C	ENSP00000418951.1:n.530-367T>C
ENST00000477382.1:c.*244T>C	ENSP00000419008.1:n.*244T>C
ENST00000486393.5:c.*488T>C	ENSP00000419868.1:n.*488T>C
ENST00000489173.1:n.1419T>C
NM_001144951.1:c.*244T>C	NP_001138423.1:n.*244T>C
NM_145262.3:c.1125T>C	NP_660305.2:p.His375=
NR_026699.1:n.1223T>C
NR_026700.1:n.695+110T>C
NR_026701.1:n.1221T>C
NR_026702.1:n.626-367T>C
XM_005264878.2:c.*244T>C	XP_005264935.1:n.*244T>C
XR_245095.2:n.2742+110T>C
XM_017005730.1:c.744T>C	XP_016861219.1:p.His248=
XM_024453351.1:c.1125T>C	XP_024309119.1:p.His375=
XM_024453352.1:c.*244T>C	XP_024309120.1:n.*244T>C
XR_001740022.2:n.3027T>C
XR_001740023.2:n.2917+110T>C
XR_245095.4:n.2743+110T>C
NM_145262.4:c.1125T>C MANE Select	NP_660305.2:p.His375=
NR_026699.2:n.1215T>C
NR_026700.2:n.687+110T>C
NR_026701.2:n.1213T>C
NR_026702.2:n.618-367T>C
NM_001144951.2:c.*244T>C	NP_001138423.1:n.*244T>C