Canonical Allele Identifier: CA408543861

Gene: HCK

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32101483C>A , CM000682.2:g.32101483C>A	GRCh38
NC_000020.10:g.30689286C>A , CM000682.1:g.30689286C>A	GRCh37
NC_000020.9:g.30152947C>A	NCBI36
NG_029471.1:g.54296C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002110.5:c.1545C>A MANE Select	NP_002101.2:p.Tyr515Ter
ENST00000375852.5:c.1545C>A MANE Select	ENSP00000365012.3:p.Tyr515Ter
NM_001172129.1:c.1482C>A	NP_001165600.1:p.Tyr494Ter
NM_001172129.2:c.1482C>A	NP_001165600.1:p.Tyr494Ter
NM_001172129.3:c.1482C>A	NP_001165600.1:p.Tyr494Ter
NM_001172130.1:c.1542C>A	NP_001165601.1:p.Tyr514Ter
NM_001172130.2:c.1542C>A	NP_001165601.1:p.Tyr514Ter
NM_001172130.3:c.1542C>A	NP_001165601.1:p.Tyr514Ter
NM_001172131.1:c.1479C>A	NP_001165602.1:p.Tyr493Ter
NM_001172131.2:c.1479C>A	NP_001165602.1:p.Tyr493Ter
NM_001172131.3:c.1479C>A	NP_001165602.1:p.Tyr493Ter
NM_001172132.1:c.1485C>A	NP_001165603.1:p.Tyr495Ter
NM_001172132.2:c.1485C>A	NP_001165603.1:p.Tyr495Ter
NM_001172132.3:c.1485C>A	NP_001165603.1:p.Tyr495Ter
NM_001172133.1:c.1482C>A	NP_001165604.1:p.Tyr494Ter
NM_001172133.2:c.1482C>A	NP_001165604.1:p.Tyr494Ter
NM_001172133.3:c.1482C>A	NP_001165604.1:p.Tyr494Ter
NM_002110.3:c.1545C>A	NP_002101.2:p.Tyr515Ter
NM_002110.4:c.1545C>A	NP_002101.2:p.Tyr515Ter
ENST00000262651.3:c.*1485C>A	ENSP00000262651.3:n.*1485C>A
ENST00000262651.4:c.*1485C>A	ENSP00000262651.4:n.*1485C>A
ENST00000375852.2:c.1545C>A	ENSP00000365012.2:p.Tyr515Ter
ENST00000375862.6:c.1542C>A	ENSP00000365022.2:p.Tyr514Ter
ENST00000375862.7:c.1542C>A	ENSP00000365022.3:p.Tyr514Ter
ENST00000486475.5:c.*1423C>A	ENSP00000420457.1:n.*1423C>A
ENST00000486475.6:c.*1423C>A	ENSP00000420457.2:n.*1423C>A
ENST00000518730.5:c.1479C>A	ENSP00000427757.1:p.Tyr493Ter
ENST00000520553.5:c.1482C>A	ENSP00000429848.1:p.Tyr494Ter
ENST00000534862.5:c.1545C>A	ENSP00000444986.2:p.Tyr515Ter
ENST00000538448.5:c.1482C>A	ENSP00000441169.1:p.Tyr494Ter
ENST00000629881.2:c.1482C>A	ENSP00000486627.1:p.Tyr494Ter