Canonical Allele Identifier: CA353076994

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327149A>C (hg19) ; chr3:g.52293133A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293133A>C , CM000665.2:g.52293133A>C	GRCh38
NC_000003.11:g.52327149A>C , CM000665.1:g.52327149A>C	GRCh37
NC_000003.10:g.52302189A>C	NCBI36
NG_023246.1:g.10314A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*7A>C MANE Select	ENSP00000389175.2:n.*7A>C
ENST00000436784.6:c.*7A>C	ENSP00000389175.2:n.*7A>C
ENST00000461183.5:c.851A>C	ENSP00000417264.1:p.Ter284Ser
ENST00000471180.5:c.722A>C	ENSP00000417526.1:p.Ter241Ser
ENST00000473032.5:c.617A>C	ENSP00000418951.1:p.Ter206Ser
ENST00000486393.5:c.*942A>C	ENSP00000419868.1:n.*942A>C
ENST00000489173.1:n.1873A>C
NM_145262.3:c.*7A>C	NP_660305.2:n.*7A>C
NR_026699.1:n.1677A>C
NR_026700.1:n.783A>C
NR_026701.1:n.1675A>C
NR_026702.1:n.713A>C
XM_005264878.2:c.*698A>C	XP_005264935.1:n.*698A>C
XR_245095.2:n.2830A>C
XM_017005730.1:c.*7A>C	XP_016861219.1:n.*7A>C
XM_024453351.1:c.*7A>C	XP_024309119.1:n.*7A>C
XM_024453352.1:c.*698A>C	XP_024309120.1:n.*698A>C
XR_001740022.2:n.3481A>C
XR_001740023.2:n.3005A>C
XR_245095.4:n.2831A>C
NM_145262.4:c.*7A>C MANE Select	NP_660305.2:n.*7A>C
NR_026699.2:n.1669A>C
NR_026700.2:n.775A>C
NR_026701.2:n.1667A>C
NR_026702.2:n.705A>C
NM_001144951.2:c.*698A>C	NP_001138423.1:n.*698A>C