Canonical Allele Identifier: CA1364789269

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293131A= , CM000665.2:g.52293131A=	GRCh38
NC_000003.11:g.52327147A= , CM000665.1:g.52327147A=	GRCh37
NC_000003.10:g.52302187A=	NCBI36
NG_023246.1:g.10312A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*5A= MANE Select	ENSP00000389175.2:n.*5A=
ENST00000436784.6:c.*5A=	ENSP00000389175.2:n.*5A=
ENST00000461183.5:c.849A=	ENSP00000417264.1:p.Ala283=
ENST00000471180.5:c.720A=	ENSP00000417526.1:p.Ala240=
ENST00000473032.5:c.615A=	ENSP00000418951.1:p.Ala205=
ENST00000486393.5:c.*940A=	ENSP00000419868.1:n.*940A=
ENST00000489173.1:n.1871A=
NM_145262.3:c.*5A=	NP_660305.2:n.*5A=
NR_026699.1:n.1675A=
NR_026700.1:n.781A=
NR_026701.1:n.1673A=
NR_026702.1:n.711A=
XM_005264878.2:c.*696A=	XP_005264935.1:n.*696A=
XR_245095.2:n.2828A=
XM_017005730.1:c.*5A=	XP_016861219.1:n.*5A=
XM_024453351.1:c.*5A=	XP_024309119.1:n.*5A=
XM_024453352.1:c.*696A=	XP_024309120.1:n.*696A=
XR_001740022.2:n.3479A=
XR_001740023.2:n.3003A=
XR_245095.4:n.2829A=
NM_145262.4:c.*5A= MANE Select	NP_660305.2:n.*5A=
NR_026699.2:n.1667A=
NR_026700.2:n.773A=
NR_026701.2:n.1665A=
NR_026702.2:n.703A=
NM_001144951.2:c.*696A=	NP_001138423.1:n.*696A=