Canonical Allele Identifier: CA1748103973

Gene: AGK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.141649163T= , CM000669.2:g.141649163T=	GRCh38
NC_000007.13:g.141348963T= , CM000669.1:g.141348963T=	GRCh37
NC_000007.12:g.140995432T=	NCBI36
NG_032079.1:g.102886T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647568.1:c.*939-100T=	ENSP00000497039.1:n.*939-100T=
ENST00000648068.1:c.976-100T=	ENSP00000498112.1:n.976-100T=
ENST00000648395.1:c.700-100T=	ENSP00000497666.1:n.700-100T=
ENST00000648489.1:n.1007-100T=
ENST00000649014.1:c.*251-100T=	ENSP00000497984.1:n.*251-100T=
ENST00000649286.2:c.976-100T= MANE Select	ENSP00000497280.1:n.976-100T=
ENST00000649365.1:c.*984-100T=	ENSP00000496835.1:n.*984-100T=
ENST00000649790.1:c.*412-100T=	ENSP00000498193.1:n.*412-100T=
ENST00000649914.1:c.964-100T=	ENSP00000497848.1:n.964-100T=
ENST00000650006.1:c.976-100T=	ENSP00000497457.1:n.976-100T=
ENST00000650365.1:c.*861-100T=	ENSP00000497358.1:n.*861-100T=
ENST00000650547.1:c.976-100T=	ENSP00000496789.1:n.976-100T=
ENST00000355413.8:c.976-100T=	ENSP00000347581.4:n.976-100T=
ENST00000473247.5:c.892-100T=	ENSP00000420776.1:n.892-100T=
ENST00000494053.1:n.33T=
ENST00000494688.1:c.*81-100T=	ENSP00000418101.1:n.*81-100T=
ENST00000629555.2:c.*81-100T=	ENSP00000487274.1:n.*81-100T=
NM_018238.3:c.976-100T=	NP_060708.1:n.976-100T=
XM_005250023.3:c.976-100T=	XP_005250080.1:n.976-100T=
XM_011516397.1:c.976-100T=	XP_011514699.1:n.976-100T=
NM_001364948.1:c.976-100T=	NP_001351877.1:n.976-100T=
NM_018238.4:c.976-100T= MANE Select	NP_060708.1:n.976-100T=
XM_011516397.3:c.976-100T=	XP_011514699.1:n.976-100T=
XM_024446835.1:c.976-100T=	XP_024302603.1:n.976-100T=
NM_001364948.2:c.976-100T=	NP_001351877.1:n.976-100T=
NM_001364948.3:c.976-100T=	NP_001351877.1:n.976-100T=