Canonical Allele Identifier: CA353074703

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52326602G>C (hg19) ; chr3:g.52292586G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292586G>C , CM000665.2:g.52292586G>C	GRCh38
NC_000003.11:g.52326602G>C , CM000665.1:g.52326602G>C	GRCh37
NC_000003.10:g.52301642G>C	NCBI36
NG_023246.1:g.9767G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1032G>C MANE Select	ENSP00000389175.2:p.Met344Ile
ENST00000305690.12:c.*151G>C	ENSP00000301965.9:n.*151G>C
ENST00000436784.6:c.1032G>C	ENSP00000389175.2:p.Met344Ile
ENST00000461183.5:c.763+17G>C	ENSP00000417264.1:n.763+17G>C
ENST00000471180.5:c.634+17G>C	ENSP00000417526.1:n.634+17G>C
ENST00000473032.5:c.530-460G>C	ENSP00000418951.1:n.530-460G>C
ENST00000477382.1:c.*151G>C	ENSP00000419008.1:n.*151G>C
ENST00000486393.5:c.*395G>C	ENSP00000419868.1:n.*395G>C
ENST00000489173.1:n.1326G>C
NM_001144951.1:c.*151G>C	NP_001138423.1:n.*151G>C
NM_145262.3:c.1032G>C	NP_660305.2:p.Met344Ile
NR_026699.1:n.1130G>C
NR_026700.1:n.695+17G>C
NR_026701.1:n.1128G>C
NR_026702.1:n.626-460G>C
XM_005264878.2:c.*151G>C	XP_005264935.1:n.*151G>C
XR_245095.2:n.2742+17G>C
XM_017005730.1:c.651G>C	XP_016861219.1:p.Met217Ile
XM_024453351.1:c.1032G>C	XP_024309119.1:p.Met344Ile
XM_024453352.1:c.*151G>C	XP_024309120.1:n.*151G>C
XR_001740022.2:n.2934G>C
XR_001740023.2:n.2917+17G>C
XR_245095.4:n.2743+17G>C
NM_145262.4:c.1032G>C MANE Select	NP_660305.2:p.Met344Ile
NR_026699.2:n.1122G>C
NR_026700.2:n.687+17G>C
NR_026701.2:n.1120G>C
NR_026702.2:n.618-460G>C
NM_001144951.2:c.*151G>C	NP_001138423.1:n.*151G>C