Canonical Allele Identifier: CA1748088805

Gene: AGK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.141611232T= , CM000669.2:g.141611232T=	GRCh38
NC_000007.13:g.141311032T= , CM000669.1:g.141311032T=	GRCh37
NC_000007.12:g.140957501T=	NCBI36
NG_032079.1:g.64955T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647568.1:c.335T=	ENSP00000497039.1:p.Leu112=
ENST00000647898.1:n.225T=
ENST00000648068.1:c.335T=	ENSP00000498112.1:p.Leu112=
ENST00000648395.1:c.59T=	ENSP00000497666.1:p.Leu20=
ENST00000648489.1:n.366T=
ENST00000648690.1:c.59T=	ENSP00000497945.1:p.Leu20=
ENST00000649014.1:c.335T=	ENSP00000497984.1:p.Leu112=
ENST00000649286.2:c.335T= MANE Select	ENSP00000497280.1:p.Leu112=
ENST00000649365.1:c.*343T=	ENSP00000496835.1:n.*343T=
ENST00000649538.1:n.363T=
ENST00000649790.1:c.59T=	ENSP00000498193.1:p.Leu20=
ENST00000649914.1:c.323T=	ENSP00000497848.1:p.Leu108=
ENST00000650006.1:c.335T=	ENSP00000497457.1:p.Leu112=
ENST00000650365.1:c.*220T=	ENSP00000497358.1:n.*220T=
ENST00000650547.1:c.335T=	ENSP00000496789.1:p.Leu112=
ENST00000355413.8:c.335T=	ENSP00000347581.4:p.Leu112=
ENST00000465241.5:n.346T=
ENST00000473247.5:c.251T=	ENSP00000420776.1:p.Leu84=
ENST00000473884.5:c.*154T=	ENSP00000420540.1:n.*154T=
ENST00000494688.1:c.326T=	ENSP00000418101.1:p.Leu109=
ENST00000496273.1:n.98T=
ENST00000629555.2:c.326T=	ENSP00000487274.1:p.Leu109=
NM_018238.3:c.335T=	NP_060708.1:p.Leu112=
XM_005250023.3:c.335T=	XP_005250080.1:p.Leu112=
XM_011516397.1:c.335T=	XP_011514699.1:p.Leu112=
NM_001364948.1:c.335T=	NP_001351877.1:p.Leu112=
NM_018238.4:c.335T= MANE Select	NP_060708.1:p.Leu112=
XM_011516397.3:c.335T=	XP_011514699.1:p.Leu112=
XM_024446835.1:c.335T=	XP_024302603.1:p.Leu112=
NM_001364948.2:c.335T=	NP_001351877.1:p.Leu112=
NM_001364948.3:c.335T=	NP_001351877.1:p.Leu112=