Canonical Allele Identifier: CA6147962

Gene: CHKA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68120954G>A , CM000673.2:g.68120954G>A	GRCh38
NC_000011.9:g.67888421G>A , CM000673.1:g.67888421G>A	GRCh37
NC_000011.8:g.67644997G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001277.3:c.224C>T MANE Select	NP_001268.2:p.Pro75Leu
ENST00000265689.9:c.224C>T MANE Select	ENSP00000265689.4:p.Pro75Leu
NM_001277.2:c.224C>T	NP_001268.2:p.Pro75Leu
NM_001376219.1:c.224C>T	NP_001363148.1:p.Pro75Leu
NM_001376220.1:c.224C>T	NP_001363149.1:p.Pro75Leu
NM_001376221.1:c.-141C>T	NP_001363150.1:n.-141C>T
NM_001376222.1:c.-141C>T	NP_001363151.1:n.-141C>T
NM_212469.1:c.224C>T	NP_997634.1:p.Pro75Leu
NM_212469.2:c.224C>T	NP_997634.1:p.Pro75Leu
NR_164782.1:n.435C>T
ENST00000265689.8:c.224C>T	ENSP00000265689.4:p.Pro75Leu
ENST00000356135.9:c.224C>T	ENSP00000348454.4:p.Pro75Leu
XM_017017147.1:c.224C>T	XP_016872636.1:p.Pro75Leu
XR_002957119.1:n.436C>T
XR_428904.2:n.435C>T
XR_428904.3:n.436C>T
XR_949772.1:n.435C>T
XR_949772.2:n.418C>T
XR_949773.1:n.435C>T
XR_949773.2:n.436C>T
XR_949777.1:n.435C>T