Canonical Allele Identifier: CA353075142

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52326682A>C (hg19) ; chr3:g.52292666A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292666A>C , CM000665.2:g.52292666A>C	GRCh38
NC_000003.11:g.52326682A>C , CM000665.1:g.52326682A>C	GRCh37
NC_000003.10:g.52301722A>C	NCBI36
NG_023246.1:g.9847A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1112A>C MANE Select	ENSP00000389175.2:p.Asp371Ala
ENST00000305690.12:c.*231A>C	ENSP00000301965.9:n.*231A>C
ENST00000436784.6:c.1112A>C	ENSP00000389175.2:p.Asp371Ala
ENST00000461183.5:c.763+97A>C	ENSP00000417264.1:n.763+97A>C
ENST00000471180.5:c.634+97A>C	ENSP00000417526.1:n.634+97A>C
ENST00000473032.5:c.530-380A>C	ENSP00000418951.1:n.530-380A>C
ENST00000477382.1:c.*231A>C	ENSP00000419008.1:n.*231A>C
ENST00000486393.5:c.*475A>C	ENSP00000419868.1:n.*475A>C
ENST00000489173.1:n.1406A>C
NM_001144951.1:c.*231A>C	NP_001138423.1:n.*231A>C
NM_145262.3:c.1112A>C	NP_660305.2:p.Asp371Ala
NR_026699.1:n.1210A>C
NR_026700.1:n.695+97A>C
NR_026701.1:n.1208A>C
NR_026702.1:n.626-380A>C
XM_005264878.2:c.*231A>C	XP_005264935.1:n.*231A>C
XR_245095.2:n.2742+97A>C
XM_017005730.1:c.731A>C	XP_016861219.1:p.Asp244Ala
XM_024453351.1:c.1112A>C	XP_024309119.1:p.Asp371Ala
XM_024453352.1:c.*231A>C	XP_024309120.1:n.*231A>C
XR_001740022.2:n.3014A>C
XR_001740023.2:n.2917+97A>C
XR_245095.4:n.2743+97A>C
NM_145262.4:c.1112A>C MANE Select	NP_660305.2:p.Asp371Ala
NR_026699.2:n.1202A>C
NR_026700.2:n.687+97A>C
NR_026701.2:n.1200A>C
NR_026702.2:n.618-380A>C
NM_001144951.2:c.*231A>C	NP_001138423.1:n.*231A>C