Canonical Allele Identifier: CA578277905

Gene: AGK

Linked Data

• dbSNP Id: rs1393607367
• gnomAD v2: 7-141349049-C-A
• gnomAD v4: 7-141649249-C-A
• MyVariant Identifiers: chr7:g.141349049C>A (hg19) ; chr7:g.141649249C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.141649249C>A , CM000669.2:g.141649249C>A	GRCh38
NC_000007.13:g.141349049C>A , CM000669.1:g.141349049C>A	GRCh37
NC_000007.12:g.140995518C>A	NCBI36
NG_032079.1:g.102972C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647568.1:c.*939-14C>A	ENSP00000497039.1:n.*939-14C>A
ENST00000648068.1:c.976-14C>A	ENSP00000498112.1:n.976-14C>A
ENST00000648395.1:c.700-14C>A	ENSP00000497666.1:n.700-14C>A
ENST00000648489.1:n.1007-14C>A
ENST00000649014.1:c.*251-14C>A	ENSP00000497984.1:n.*251-14C>A
ENST00000649286.2:c.976-14C>A MANE Select	ENSP00000497280.1:n.976-14C>A
ENST00000649365.1:c.*984-14C>A	ENSP00000496835.1:n.*984-14C>A
ENST00000649790.1:c.*412-14C>A	ENSP00000498193.1:n.*412-14C>A
ENST00000649914.1:c.964-14C>A	ENSP00000497848.1:n.964-14C>A
ENST00000650006.1:c.976-14C>A	ENSP00000497457.1:n.976-14C>A
ENST00000650365.1:c.*861-14C>A	ENSP00000497358.1:n.*861-14C>A
ENST00000650547.1:c.976-14C>A	ENSP00000496789.1:n.976-14C>A
ENST00000355413.8:c.976-14C>A	ENSP00000347581.4:n.976-14C>A
ENST00000473247.5:c.892-14C>A	ENSP00000420776.1:n.892-14C>A
ENST00000494053.1:n.119C>A
ENST00000494688.1:c.*81-14C>A	ENSP00000418101.1:n.*81-14C>A
ENST00000629555.2:c.*81-14C>A	ENSP00000487274.1:n.*81-14C>A
NM_018238.3:c.976-14C>A	NP_060708.1:n.976-14C>A
XM_005250023.3:c.976-14C>A	XP_005250080.1:n.976-14C>A
XM_011516397.1:c.976-14C>A	XP_011514699.1:n.976-14C>A
NM_001364948.1:c.976-14C>A	NP_001351877.1:n.976-14C>A
NM_018238.4:c.976-14C>A MANE Select	NP_060708.1:n.976-14C>A
XM_011516397.3:c.976-14C>A	XP_011514699.1:n.976-14C>A
XM_024446835.1:c.976-14C>A	XP_024302603.1:n.976-14C>A
NM_001364948.2:c.976-14C>A	NP_001351877.1:n.976-14C>A
NM_001364948.3:c.976-14C>A	NP_001351877.1:n.976-14C>A