Canonical Allele Identifier: CA2354251882

Gene: CRNKL1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.20052443G= , CM000682.2:g.20052443G=	GRCh38
NC_000020.10:g.20033087G= , CM000682.1:g.20033087G=	GRCh37
NC_000020.9:g.19981087G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001278628.2:c.-101C= MANE Select	NP_001265557.1:n.-101C=
ENST00000536226.2:c.-101C= MANE Select	ENSP00000440733.1:n.-101C=
NM_001278625.1:c.347C=	NP_001265554.1:p.Ser116=
NM_001278625.2:c.347C=	NP_001265554.1:p.Ser116=
NM_001278626.1:c.-319+36C=	NP_001265555.1:n.-319+36C=
NM_001278626.2:c.-319+36C=	NP_001265555.1:n.-319+36C=
NM_001278627.1:c.-319+32C=	NP_001265556.1:n.-319+32C=
NM_001278627.2:c.-319+32C=	NP_001265556.1:n.-319+32C=
NM_001278628.1:c.-101C=	NP_001265557.1:n.-101C=
NM_016652.5:c.383C=	NP_057736.4:p.Ser128=
NM_016652.6:c.383C=	NP_057736.4:p.Ser128=
ENST00000377327.8:c.347C=	ENSP00000366544.4:p.Ser116=
ENST00000377340.6:c.383C=	ENSP00000366557.2:p.Ser128=
ENST00000490910.5:c.311+36C=	ENSP00000429226.1:n.311+36C=
ENST00000496549.5:c.221+32C=	ENSP00000428436.1:n.221+32C=
ENST00000536226.1:c.-101C=	ENSP00000440733.1:n.-101C=