Canonical Allele Identifier: CA1364789064

Gene: GLYCTK

Linked Data

• dbSNP Id: rs1700520954

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292714_52292716del , CM000665.2:g.52292714_52292716del	GRCh38
NC_000003.11:g.52326730_52326732del , CM000665.1:g.52326730_52326732del	GRCh37
NC_000003.10:g.52301770_52301772del	NCBI36
NG_023246.1:g.9895_9897del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1160_1162del MANE Select	ENSP00000389175.2:p.Gln387del
ENST00000305690.12:c.*279_*281del	ENSP00000301965.9:n.*279_*281del
ENST00000436784.6:c.1160_1162del	ENSP00000389175.2:p.Gln387del
ENST00000461183.5:c.763+145_763+147del	ENSP00000417264.1:n.763+145_763+147del
ENST00000471180.5:c.634+145_634+147del	ENSP00000417526.1:n.634+145_634+147del
ENST00000473032.5:c.530-332_530-330del	ENSP00000418951.1:n.530-332_530-330del
ENST00000477382.1:c.*279_*281del	ENSP00000419008.1:n.*279_*281del
ENST00000486393.5:c.*523_*525del	ENSP00000419868.1:n.*523_*525del
ENST00000489173.1:n.1454_1456del
NM_001144951.1:c.*279_*281del	NP_001138423.1:n.*279_*281del
NM_145262.3:c.1160_1162del	NP_660305.2:p.Gln387del
NR_026699.1:n.1258_1260del
NR_026700.1:n.695+145_695+147del
NR_026701.1:n.1256_1258del
NR_026702.1:n.626-332_626-330del
XM_005264878.2:c.*279_*281del	XP_005264935.1:n.*279_*281del
XR_245095.2:n.2742+145_2742+147del
XM_017005730.1:c.779_781del	XP_016861219.1:p.Gln260del
XM_024453351.1:c.1160_1162del	XP_024309119.1:p.Gln387del
XM_024453352.1:c.*279_*281del	XP_024309120.1:n.*279_*281del
XR_001740022.2:n.3062_3064del
XR_001740023.2:n.2917+145_2917+147del
XR_245095.4:n.2743+145_2743+147del
NM_145262.4:c.1160_1162del MANE Select	NP_660305.2:p.Gln387del
NR_026699.2:n.1250_1252del
NR_026700.2:n.687+145_687+147del
NR_026701.2:n.1248_1250del
NR_026702.2:n.618-332_618-330del
NM_001144951.2:c.*279_*281del	NP_001138423.1:n.*279_*281del