Canonical Allele Identifier: CA457988679

Gene: AGK

Linked Data

• MyVariant Identifiers: chr7:g.141349065C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.141649265C>T , CM000669.2:g.141649265C>T	GRCh38
NC_000007.13:g.141349065C>T , CM000669.1:g.141349065C>T	GRCh37
NC_000007.12:g.140995534C>T	NCBI36
NG_032079.1:g.102988C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647568.1:c.*941C>T	ENSP00000497039.1:n.*941C>T
ENST00000648068.1:c.978C>T	ENSP00000498112.1:p.Ser326=
ENST00000648395.1:c.702C>T	ENSP00000497666.1:p.Ser234=
ENST00000648489.1:n.1009C>T
ENST00000649014.1:c.*253C>T	ENSP00000497984.1:n.*253C>T
ENST00000649286.2:c.978C>T MANE Select	ENSP00000497280.1:p.Ser326=
ENST00000649365.1:c.*986C>T	ENSP00000496835.1:n.*986C>T
ENST00000649790.1:c.*414C>T	ENSP00000498193.1:n.*414C>T
ENST00000649914.1:c.966C>T	ENSP00000497848.1:p.Ser322=
ENST00000650006.1:c.978C>T	ENSP00000497457.1:p.Ser326=
ENST00000650365.1:c.*863C>T	ENSP00000497358.1:n.*863C>T
ENST00000650547.1:c.978C>T	ENSP00000496789.1:p.Ser326=
ENST00000355413.8:c.978C>T	ENSP00000347581.4:p.Ser326=
ENST00000473247.5:c.894C>T	ENSP00000420776.1:p.Ser298=
ENST00000494053.1:n.135C>T
ENST00000494688.1:c.*83C>T	ENSP00000418101.1:n.*83C>T
ENST00000629555.2:c.*83C>T	ENSP00000487274.1:n.*83C>T
NM_018238.3:c.978C>T	NP_060708.1:p.Ser326=
XM_005250023.3:c.978C>T	XP_005250080.1:p.Ser326=
XM_011516397.1:c.978C>T	XP_011514699.1:p.Ser326=
NM_001364948.1:c.978C>T	NP_001351877.1:p.Ser326=
NM_018238.4:c.978C>T MANE Select	NP_060708.1:p.Ser326=
XM_011516397.3:c.978C>T	XP_011514699.1:p.Ser326=
XM_024446835.1:c.978C>T	XP_024302603.1:p.Ser326=
NM_001364948.2:c.978C>T	NP_001351877.1:p.Ser326=
NM_001364948.3:c.978C>T	NP_001351877.1:p.Ser326=