Canonical Allele Identifier: CA10579434

Gene: CDK4 TSPAN31

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57749273G>T , CM000674.2:g.57749273G>T	GRCh38
NC_000012.11:g.58143056G>T , CM000674.1:g.58143056G>T	GRCh37
NC_000012.10:g.56429323G>T	NCBI36
NG_007484.2:g.8109C>A , LRG_490:g.8109C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257904.11:c.728C>A (CDK4) MANE Select	ENSP00000257904.5:p.Ser243Tyr
ENST00000257910.8:c.*1983G>T (TSPAN31) MANE Select	ENSP00000257910.3:n.*1983G>T
ENST00000257904.10:c.728C>A (CDK4)	ENSP00000257904.5:p.Ser243Tyr
ENST00000312990.10:c.*40C>A (CDK4)	ENSP00000316889.6:n.*40C>A
ENST00000546489.5:c.506C>A (CDK4)	ENSP00000447779.1:p.Ser169Tyr
ENST00000547281.5:c.506C>A (CDK4)	ENSP00000447274.1:p.Ser169Tyr
ENST00000547992.5:c.*1983G>T (TSPAN31)	ENSP00000448209.1:n.*1983G>T
ENST00000549606.5:c.-62C>A (CDK4)	ENSP00000447005.1:n.-62C>A
ENST00000550419.5:c.*134C>A (CDK4)	ENSP00000448098.1:n.*134C>A
ENST00000551888.5:n.554C>A (CDK4)
ENST00000552713.5:n.387C>A (CDK4)
ENST00000553237.5:c.*367C>A (CDK4)	ENSP00000448885.1:n.*367C>A
NM_000075.3:c.728C>A (CDK4)	NP_000066.1:p.Ser243Tyr
NM_000075.4:c.728C>A (CDK4) MANE Select	NP_000066.1:p.Ser243Tyr
NM_005981.5:c.*1983G>T (TSPAN31) MANE Select	NP_005972.1:n.*1983G>T
NM_001330168.2:c.*1983G>T (TSPAN31)	NP_001317097.1:n.*1983G>T
NM_001330169.2:c.*1983G>T (TSPAN31)	NP_001317098.1:n.*1983G>T