Canonical Allele Identifier: CA1585606881

Gene: MYOT PKD2L2-DT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137870741C= , CM000667.2:g.137870741C=	GRCh38
NC_000005.9:g.137206430C= , CM000667.1:g.137206430C=	GRCh37
NC_000005.8:g.137234329C=	NCBI36
NG_008894.1:g.7886C= , LRG_201:g.7886C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239926.9:c.90C= (MYOT) MANE Select	ENSP00000239926.4:p.Ser30=
ENST00000239926.8:c.90C= (MYOT)	ENSP00000239926.4:p.Ser30=
ENST00000421631.6:c.-197+216C= (MYOT)	ENSP00000391185.2:n.-197+216C=
ENST00000509812.5:n.179+216C= (MYOT)
ENST00000511625.5:n.179+216C= (MYOT)
ENST00000515645.1:c.-120-136C= (MYOT)	ENSP00000426281.1:n.-120-136C=
NM_001135940.1:c.-197+216C= (MYOT)	NP_001129412.1:n.-197+216C=
NM_001300911.1:c.-120-136C= (MYOT)	NP_001287840.1:n.-120-136C=
NM_006790.2:c.90C= , LRG_201t1:c.90C= (MYOT)	NP_006781.1:p.Ser30=
XR_948815.1:n.220-11478G= (PKD2L2-DT)
XR_948816.1:n.58-11478G= (PKD2L2-DT)
XM_017010060.1:c.-355-136C= (MYOT)	XP_016865549.1:n.-355-136C=
XM_017010061.1:c.-491C= (MYOT)	XP_016865550.1:n.-491C=
XM_017010062.1:c.-225+216C= (MYOT)	XP_016865551.1:n.-225+216C=
XR_948815.2:n.347-11478G= (PKD2L2-DT)
NM_001135940.2:c.-197+216C= (MYOT)	NP_001129412.1:n.-197+216C=
NM_001300911.2:c.-120-136C= (MYOT)	NP_001287840.1:n.-120-136C=
NM_006790.3:c.90C= (MYOT) MANE Select	NP_006781.1:p.Ser30=