Canonical Allele Identifier: CA353076600

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327072A>C (hg19) ; chr3:g.52293056A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293056A>C , CM000665.2:g.52293056A>C	GRCh38
NC_000003.11:g.52327072A>C , CM000665.1:g.52327072A>C	GRCh37
NC_000003.10:g.52302112A>C	NCBI36
NG_023246.1:g.10237A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000436784.7:c.1502A>C MANE Select	ENSP00000389175.2:p.His501Pro
ENST00000436784.6:c.1502A>C	ENSP00000389175.2:p.His501Pro
ENST00000461183.5:c.774A>C	ENSP00000417264.1:p.Thr258=
ENST00000471180.5:c.645A>C	ENSP00000417526.1:p.Thr215=
ENST00000473032.5:c.540A>C	ENSP00000418951.1:p.Thr180=
ENST00000486393.5:c.*865A>C	ENSP00000419868.1:n.*865A>C
ENST00000489173.1:n.1796A>C
NM_145262.3:c.1502A>C	NP_660305.2:p.His501Pro
NR_026699.1:n.1600A>C
NR_026700.1:n.706A>C
NR_026701.1:n.1598A>C
NR_026702.1:n.636A>C
XM_005264878.2:c.*621A>C	XP_005264935.1:n.*621A>C
XR_245095.2:n.2753A>C
XM_017005730.1:c.1121A>C	XP_016861219.1:p.His374Pro
XM_024453351.1:c.1502A>C	XP_024309119.1:p.His501Pro
XM_024453352.1:c.*621A>C	XP_024309120.1:n.*621A>C
XR_001740022.2:n.3404A>C
XR_001740023.2:n.2928A>C
XR_245095.4:n.2754A>C
NM_145262.4:c.1502A>C MANE Select	NP_660305.2:p.His501Pro
NR_026699.2:n.1592A>C
NR_026700.2:n.698A>C
NR_026701.2:n.1590A>C
NR_026702.2:n.628A>C
NM_001144951.2:c.*621A>C	NP_001138423.1:n.*621A>C