Canonical Allele Identifier: CA353075358

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52326730A>C (hg19) ; chr3:g.52292714A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292714A>C , CM000665.2:g.52292714A>C	GRCh38
NC_000003.11:g.52326730A>C , CM000665.1:g.52326730A>C	GRCh37
NC_000003.10:g.52301770A>C	NCBI36
NG_023246.1:g.9895A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1160A>C MANE Select	ENSP00000389175.2:p.Gln387Pro
ENST00000305690.12:c.*279A>C	ENSP00000301965.9:n.*279A>C
ENST00000436784.6:c.1160A>C	ENSP00000389175.2:p.Gln387Pro
ENST00000461183.5:c.763+145A>C	ENSP00000417264.1:n.763+145A>C
ENST00000471180.5:c.634+145A>C	ENSP00000417526.1:n.634+145A>C
ENST00000473032.5:c.530-332A>C	ENSP00000418951.1:n.530-332A>C
ENST00000477382.1:c.*279A>C	ENSP00000419008.1:n.*279A>C
ENST00000486393.5:c.*523A>C	ENSP00000419868.1:n.*523A>C
ENST00000489173.1:n.1454A>C
NM_001144951.1:c.*279A>C	NP_001138423.1:n.*279A>C
NM_145262.3:c.1160A>C	NP_660305.2:p.Gln387Pro
NR_026699.1:n.1258A>C
NR_026700.1:n.695+145A>C
NR_026701.1:n.1256A>C
NR_026702.1:n.626-332A>C
XM_005264878.2:c.*279A>C	XP_005264935.1:n.*279A>C
XR_245095.2:n.2742+145A>C
XM_017005730.1:c.779A>C	XP_016861219.1:p.Gln260Pro
XM_024453351.1:c.1160A>C	XP_024309119.1:p.Gln387Pro
XM_024453352.1:c.*279A>C	XP_024309120.1:n.*279A>C
XR_001740022.2:n.3062A>C
XR_001740023.2:n.2917+145A>C
XR_245095.4:n.2743+145A>C
NM_145262.4:c.1160A>C MANE Select	NP_660305.2:p.Gln387Pro
NR_026699.2:n.1250A>C
NR_026700.2:n.687+145A>C
NR_026701.2:n.1248A>C
NR_026702.2:n.618-332A>C
NM_001144951.2:c.*279A>C	NP_001138423.1:n.*279A>C