Canonical Allele Identifier: CA353076617

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327078T>C (hg19) ; chr3:g.52293062T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293062T>C , CM000665.2:g.52293062T>C	GRCh38
NC_000003.11:g.52327078T>C , CM000665.1:g.52327078T>C	GRCh37
NC_000003.10:g.52302118T>C	NCBI36
NG_023246.1:g.10243T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000436784.7:c.1508T>C MANE Select	ENSP00000389175.2:p.Leu503Pro
ENST00000436784.6:c.1508T>C	ENSP00000389175.2:p.Leu503Pro
ENST00000461183.5:c.780T>C	ENSP00000417264.1:p.Ala260=
ENST00000471180.5:c.651T>C	ENSP00000417526.1:p.Ala217=
ENST00000473032.5:c.546T>C	ENSP00000418951.1:p.Ala182=
ENST00000486393.5:c.*871T>C	ENSP00000419868.1:n.*871T>C
ENST00000489173.1:n.1802T>C
NM_145262.3:c.1508T>C	NP_660305.2:p.Leu503Pro
NR_026699.1:n.1606T>C
NR_026700.1:n.712T>C
NR_026701.1:n.1604T>C
NR_026702.1:n.642T>C
XM_005264878.2:c.*627T>C	XP_005264935.1:n.*627T>C
XR_245095.2:n.2759T>C
XM_017005730.1:c.1127T>C	XP_016861219.1:p.Leu376Pro
XM_024453351.1:c.1508T>C	XP_024309119.1:p.Leu503Pro
XM_024453352.1:c.*627T>C	XP_024309120.1:n.*627T>C
XR_001740022.2:n.3410T>C
XR_001740023.2:n.2934T>C
XR_245095.4:n.2760T>C
NM_145262.4:c.1508T>C MANE Select	NP_660305.2:p.Leu503Pro
NR_026699.2:n.1598T>C
NR_026700.2:n.704T>C
NR_026701.2:n.1596T>C
NR_026702.2:n.634T>C
NM_001144951.2:c.*627T>C	NP_001138423.1:n.*627T>C