Canonical Allele Identifier: CA2577780408

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292603_52292609del , CM000665.2:g.52292603_52292609del	GRCh38
NC_000003.11:g.52326619_52326625del , CM000665.1:g.52326619_52326625del	GRCh37
NC_000003.10:g.52301659_52301665del	NCBI36
NG_023246.1:g.9784_9790del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1049_1055del MANE Select	ENSP00000389175.2:p.Leu350ProfsTer?
ENST00000305690.12:c.*168_*174del	ENSP00000301965.9:n.*168_*174del
ENST00000436784.6:c.1049_1055del	ENSP00000389175.2:p.Leu350ProfsTer?
ENST00000461183.5:c.763+34_763+40del	ENSP00000417264.1:n.763+34_763+40del
ENST00000471180.5:c.634+34_634+40del	ENSP00000417526.1:n.634+34_634+40del
ENST00000473032.5:c.530-443_530-437del	ENSP00000418951.1:n.530-443_530-437del
ENST00000477382.1:c.*168_*174del	ENSP00000419008.1:n.*168_*174del
ENST00000486393.5:c.*412_*418del	ENSP00000419868.1:n.*412_*418del
ENST00000489173.1:n.1343_1349del
NM_001144951.1:c.*168_*174del	NP_001138423.1:n.*168_*174del
NM_145262.3:c.1049_1055del	NP_660305.2:p.Leu350ProfsTer?
NR_026699.1:n.1147_1153del
NR_026700.1:n.695+34_695+40del
NR_026701.1:n.1145_1151del
NR_026702.1:n.626-443_626-437del
XM_005264878.2:c.*168_*174del	XP_005264935.1:n.*168_*174del
XR_245095.2:n.2742+34_2742+40del
XM_017005730.1:c.668_674del	XP_016861219.1:p.Leu223ProfsTer?
XM_024453351.1:c.1049_1055del	XP_024309119.1:p.Leu350ProfsTer?
XM_024453352.1:c.*168_*174del	XP_024309120.1:n.*168_*174del
XR_001740022.2:n.2951_2957del
XR_001740023.2:n.2917+34_2917+40del
XR_245095.4:n.2743+34_2743+40del
NM_145262.4:c.1049_1055del MANE Select	NP_660305.2:p.Leu350ProfsTer?
NR_026699.2:n.1139_1145del
NR_026700.2:n.687+34_687+40del
NR_026701.2:n.1137_1143del
NR_026702.2:n.618-443_618-437del
NM_001144951.2:c.*168_*174del	NP_001138423.1:n.*168_*174del