Canonical Allele Identifier: CA4517259

Gene: AGK

Linked Data

• ClinVar Variation Id: 383284
• ClinVar RCV Id: RCV001161082 ; RCV001161083 ; RCV001703797
• dbSNP Id: rs371437227
• ExAC: 7:141255250 T / C
• gnomAD v2: 7-141255250-T-C
• gnomAD v3: 7-141555450-T-C
• gnomAD v4: 7-141555450-T-C
• MyVariant Identifiers: chr7:g.141255250T>C (hg19) ; chr7:g.141555450T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.141555450T>C , CM000669.2:g.141555450T>C	GRCh38
NC_000007.13:g.141255250T>C , CM000669.1:g.141255250T>C	GRCh37
NC_000007.12:g.140901719T>C	NCBI36
NG_032079.1:g.9173T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647568.1:c.-14-3T>C	ENSP00000497039.1:n.-14-3T>C
ENST00000648068.1:c.-14-3T>C	ENSP00000498112.1:n.-14-3T>C
ENST00000648395.1:c.-176+3951T>C	ENSP00000497666.1:n.-176+3951T>C
ENST00000648489.1:n.29-14T>C
ENST00000648690.1:c.-176+4016T>C	ENSP00000497945.1:n.-176+4016T>C
ENST00000649014.1:c.-3-14T>C	ENSP00000497984.1:n.-3-14T>C
ENST00000649286.2:c.-14-3T>C MANE Select	ENSP00000497280.1:n.-14-3T>C
ENST00000649365.1:c.-14-3T>C	ENSP00000496835.1:n.-14-3T>C
ENST00000649538.1:n.12T>C
ENST00000649790.1:c.-176+4016T>C	ENSP00000498193.1:n.-176+4016T>C
ENST00000649914.1:c.-240-3T>C	ENSP00000497848.1:n.-240-3T>C
ENST00000650006.1:c.-17T>C	ENSP00000497457.1:n.-17T>C
ENST00000650365.1:c.-14-3T>C	ENSP00000497358.1:n.-14-3T>C
ENST00000650547.1:c.-14-3T>C	ENSP00000496789.1:n.-14-3T>C
ENST00000355413.8:c.-14-3T>C	ENSP00000347581.4:n.-14-3T>C
ENST00000473247.5:c.-102-3T>C	ENSP00000420776.1:n.-102-3T>C
ENST00000473884.5:c.-14-3T>C	ENSP00000420540.1:n.-14-3T>C
ENST00000495028.5:n.26-3T>C
ENST00000629555.2:c.-14-3T>C	ENSP00000487274.1:n.-14-3T>C
NM_018238.3:c.-14-3T>C	NP_060708.1:n.-14-3T>C
XM_005250023.3:c.-14-3T>C	XP_005250080.1:n.-14-3T>C
XM_011516397.1:c.-14-3T>C	XP_011514699.1:n.-14-3T>C
NM_001364948.1:c.-14-3T>C	NP_001351877.1:n.-14-3T>C
NM_018238.4:c.-14-3T>C MANE Select	NP_060708.1:n.-14-3T>C
XM_011516397.3:c.-14-3T>C	XP_011514699.1:n.-14-3T>C
XM_024446835.1:c.-14-3T>C	XP_024302603.1:n.-14-3T>C
NM_001364948.2:c.-14-3T>C	NP_001351877.1:n.-14-3T>C
NM_001364948.3:c.-14-3T>C	NP_001351877.1:n.-14-3T>C