Canonical Allele Identifier: CA2212359971

Gene: CRYM

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.21258781T= , CM000678.2:g.21258781T=	GRCh38
NC_000016.9:g.21270102T= , CM000678.1:g.21270102T=	GRCh37
NC_000016.8:g.21177603T=	NCBI36
NG_011610.1:g.49316A=

Transcript Alleles

HGVS	Amino-acid Change
NM_001376256.1:c.945A= MANE Select	NP_001363185.1:p.Ter315=
ENST00000572914.2:c.945A= MANE Select	ENSP00000461904.2:p.Ter315=
NM_001888.4:c.945A=	NP_001879.1:p.Ter315=
NM_001888.5:c.945A=	NP_001879.1:p.Ter315=
ENST00000219599.7:c.945A=	ENSP00000219599.3:p.Ter315=
ENST00000219599.8:c.945A=	ENSP00000219599.3:p.Ter315=
ENST00000543948.5:c.945A=	ENSP00000440227.1:p.Ter315=
ENST00000570401.5:c.264+8A=
ENST00000574448.5:c.*520+2473A=	ENSP00000459982.1:n.*520+2473A=
XM_011545740.1:c.945A=	XP_011544042.1:p.Ter315=
XM_024450157.1:c.945A=	XP_024305925.1:p.Ter315=
XR_950904.1:n.735+3988T=