Canonical Allele Identifier: CA353074999

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52326657A>T (hg19) ; chr3:g.52292641A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292641A>T , CM000665.2:g.52292641A>T	GRCh38
NC_000003.11:g.52326657A>T , CM000665.1:g.52326657A>T	GRCh37
NC_000003.10:g.52301697A>T	NCBI36
NG_023246.1:g.9822A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1087A>T MANE Select	ENSP00000389175.2:p.Met363Leu
ENST00000305690.12:c.*206A>T	ENSP00000301965.9:n.*206A>T
ENST00000436784.6:c.1087A>T	ENSP00000389175.2:p.Met363Leu
ENST00000461183.5:c.763+72A>T	ENSP00000417264.1:n.763+72A>T
ENST00000471180.5:c.634+72A>T	ENSP00000417526.1:n.634+72A>T
ENST00000473032.5:c.530-405A>T	ENSP00000418951.1:n.530-405A>T
ENST00000477382.1:c.*206A>T	ENSP00000419008.1:n.*206A>T
ENST00000486393.5:c.*450A>T	ENSP00000419868.1:n.*450A>T
ENST00000489173.1:n.1381A>T
NM_001144951.1:c.*206A>T	NP_001138423.1:n.*206A>T
NM_145262.3:c.1087A>T	NP_660305.2:p.Met363Leu
NR_026699.1:n.1185A>T
NR_026700.1:n.695+72A>T
NR_026701.1:n.1183A>T
NR_026702.1:n.626-405A>T
XM_005264878.2:c.*206A>T	XP_005264935.1:n.*206A>T
XR_245095.2:n.2742+72A>T
XM_017005730.1:c.706A>T	XP_016861219.1:p.Met236Leu
XM_024453351.1:c.1087A>T	XP_024309119.1:p.Met363Leu
XM_024453352.1:c.*206A>T	XP_024309120.1:n.*206A>T
XR_001740022.2:n.2989A>T
XR_001740023.2:n.2917+72A>T
XR_245095.4:n.2743+72A>T
NM_145262.4:c.1087A>T MANE Select	NP_660305.2:p.Met363Leu
NR_026699.2:n.1177A>T
NR_026700.2:n.687+72A>T
NR_026701.2:n.1175A>T
NR_026702.2:n.618-405A>T
NM_001144951.2:c.*206A>T	NP_001138423.1:n.*206A>T