Canonical Allele Identifier: CA1364789063

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292711_52292714delinsTGCA , CM000665.2:g.52292711_52292714delinsTGCA	GRCh38
NC_000003.11:g.52326727_52326730delinsTGCA , CM000665.1:g.52326727_52326730delinsTGCA	GRCh37
NC_000003.10:g.52301767_52301770delinsTGCA	NCBI36
NG_023246.1:g.9892_9895delinsTGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1157_1160delinsTGCA MANE Select	ENSP00000389175.2:p.Leu386=
ENST00000305690.12:c.*276_*279delinsTGCA	ENSP00000301965.9:n.*276_*279delinsTGCA
ENST00000436784.6:c.1157_1160delinsTGCA	ENSP00000389175.2:p.Leu386=
ENST00000461183.5:c.763+142_763+145delinsTGCA	ENSP00000417264.1:n.763+142_763+145delinsTGCA
ENST00000471180.5:c.634+142_634+145delinsTGCA	ENSP00000417526.1:n.634+142_634+145delinsTGCA
ENST00000473032.5:c.530-335_530-332delinsTGCA	ENSP00000418951.1:n.530-335_530-332delinsTGCA
ENST00000477382.1:c.*276_*279delinsTGCA	ENSP00000419008.1:n.*276_*279delinsTGCA
ENST00000486393.5:c.*520_*523delinsTGCA	ENSP00000419868.1:n.*520_*523delinsTGCA
ENST00000489173.1:n.1451_1454delinsTGCA
NM_001144951.1:c.*276_*279delinsTGCA	NP_001138423.1:n.*276_*279delinsTGCA
NM_145262.3:c.1157_1160delinsTGCA	NP_660305.2:p.Leu386=
NR_026699.1:n.1255_1258delinsTGCA
NR_026700.1:n.695+142_695+145delinsTGCA
NR_026701.1:n.1253_1256delinsTGCA
NR_026702.1:n.626-335_626-332delinsTGCA
XM_005264878.2:c.*276_*279delinsTGCA	XP_005264935.1:n.*276_*279delinsTGCA
XR_245095.2:n.2742+142_2742+145delinsTGCA
XM_017005730.1:c.776_779delinsTGCA	XP_016861219.1:p.Leu259=
XM_024453351.1:c.1157_1160delinsTGCA	XP_024309119.1:p.Leu386=
XM_024453352.1:c.*276_*279delinsTGCA	XP_024309120.1:n.*276_*279delinsTGCA
XR_001740022.2:n.3059_3062delinsTGCA
XR_001740023.2:n.2917+142_2917+145delinsTGCA
XR_245095.4:n.2743+142_2743+145delinsTGCA
NM_145262.4:c.1157_1160delinsTGCA MANE Select	NP_660305.2:p.Leu386=
NR_026699.2:n.1247_1250delinsTGCA
NR_026700.2:n.687+142_687+145delinsTGCA
NR_026701.2:n.1245_1248delinsTGCA
NR_026702.2:n.618-335_618-332delinsTGCA
NM_001144951.2:c.*276_*279delinsTGCA	NP_001138423.1:n.*276_*279delinsTGCA