Canonical Allele Identifier: CA1585606936

Gene: MYOT PKD2L2-DT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137870842T= , CM000667.2:g.137870842T=	GRCh38
NC_000005.9:g.137206531T= , CM000667.1:g.137206531T=	GRCh37
NC_000005.8:g.137234430T=	NCBI36
NG_008894.1:g.7987T= , LRG_201:g.7987T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000239926.9:c.191T= (MYOT) MANE Select	ENSP00000239926.4:p.Met64=
ENST00000239926.8:c.191T= (MYOT)	ENSP00000239926.4:p.Met64=
ENST00000421631.6:c.-197+317T= (MYOT)	ENSP00000391185.2:n.-197+317T=
ENST00000509812.5:n.179+317T= (MYOT)
ENST00000511625.5:n.179+317T= (MYOT)
ENST00000515645.1:c.-120-35T= (MYOT)	ENSP00000426281.1:n.-120-35T=
NM_001135940.1:c.-197+317T= (MYOT)	NP_001129412.1:n.-197+317T=
NM_001300911.1:c.-120-35T= (MYOT)	NP_001287840.1:n.-120-35T=
NM_006790.2:c.191T= , LRG_201t1:c.191T= (MYOT)	NP_006781.1:p.Met64=
XR_948815.1:n.220-11579A= (PKD2L2-DT)
XR_948816.1:n.58-11579A= (PKD2L2-DT)
XM_017010060.1:c.-355-35T= (MYOT)	XP_016865549.1:n.-355-35T=
XM_017010061.1:c.-390T= (MYOT)	XP_016865550.1:n.-390T=
XM_017010062.1:c.-225+317T= (MYOT)	XP_016865551.1:n.-225+317T=
XR_948815.2:n.347-11579A= (PKD2L2-DT)
NM_001135940.2:c.-197+317T= (MYOT)	NP_001129412.1:n.-197+317T=
NM_001300911.2:c.-120-35T= (MYOT)	NP_001287840.1:n.-120-35T=
NM_006790.3:c.191T= (MYOT) MANE Select	NP_006781.1:p.Met64=