Canonical Allele Identifier: CA353075269

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52326706C>A (hg19) ; chr3:g.52292690C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292690C>A , CM000665.2:g.52292690C>A	GRCh38
NC_000003.11:g.52326706C>A , CM000665.1:g.52326706C>A	GRCh37
NC_000003.10:g.52301746C>A	NCBI36
NG_023246.1:g.9871C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1136C>A MANE Select	ENSP00000389175.2:p.Ala379Asp
ENST00000305690.12:c.*255C>A	ENSP00000301965.9:n.*255C>A
ENST00000436784.6:c.1136C>A	ENSP00000389175.2:p.Ala379Asp
ENST00000461183.5:c.763+121C>A	ENSP00000417264.1:n.763+121C>A
ENST00000471180.5:c.634+121C>A	ENSP00000417526.1:n.634+121C>A
ENST00000473032.5:c.530-356C>A	ENSP00000418951.1:n.530-356C>A
ENST00000477382.1:c.*255C>A	ENSP00000419008.1:n.*255C>A
ENST00000486393.5:c.*499C>A	ENSP00000419868.1:n.*499C>A
ENST00000489173.1:n.1430C>A
NM_001144951.1:c.*255C>A	NP_001138423.1:n.*255C>A
NM_145262.3:c.1136C>A	NP_660305.2:p.Ala379Asp
NR_026699.1:n.1234C>A
NR_026700.1:n.695+121C>A
NR_026701.1:n.1232C>A
NR_026702.1:n.626-356C>A
XM_005264878.2:c.*255C>A	XP_005264935.1:n.*255C>A
XR_245095.2:n.2742+121C>A
XM_017005730.1:c.755C>A	XP_016861219.1:p.Ala252Asp
XM_024453351.1:c.1136C>A	XP_024309119.1:p.Ala379Asp
XM_024453352.1:c.*255C>A	XP_024309120.1:n.*255C>A
XR_001740022.2:n.3038C>A
XR_001740023.2:n.2917+121C>A
XR_245095.4:n.2743+121C>A
NM_145262.4:c.1136C>A MANE Select	NP_660305.2:p.Ala379Asp
NR_026699.2:n.1226C>A
NR_026700.2:n.687+121C>A
NR_026701.2:n.1224C>A
NR_026702.2:n.618-356C>A
NM_001144951.2:c.*255C>A	NP_001138423.1:n.*255C>A