Canonical Allele Identifier: CA1585606901
Gene: MYOT HGNC NCBI
PKD2L2-DT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.137870773T= , CM000667.2:g.137870773T= GRCh38
NC_000005.9:g.137206462T= , CM000667.1:g.137206462T= GRCh37
NC_000005.8:g.137234361T= NCBI36
NG_008894.1:g.7918T= , LRG_201:g.7918T=

Transcript Alleles

HGVS Amino-acid change
ENST00000239926.9:c.122T= (MYOT) MANE Select ENSP00000239926.4:p.Ile41=
ENST00000239926.8:c.122T= (MYOT) ENSP00000239926.4:p.Ile41=
ENST00000421631.6:c.-197+248T= (MYOT) ENSP00000391185.2:n.-197+248T=
ENST00000509812.5:n.179+248T= (MYOT)
ENST00000511625.5:n.179+248T= (MYOT)
ENST00000515645.1:c.-120-104T= (MYOT) ENSP00000426281.1:n.-120-104T=
NM_001135940.1:c.-197+248T= (MYOT) NP_001129412.1:n.-197+248T=
NM_001300911.1:c.-120-104T= (MYOT) NP_001287840.1:n.-120-104T=
NM_006790.2:c.122T= , LRG_201t1:c.122T= (MYOT) NP_006781.1:p.Ile41=
XR_948815.1:n.220-11510A= (PKD2L2-DT)
XR_948816.1:n.58-11510A= (PKD2L2-DT)
XM_017010060.1:c.-355-104T= (MYOT) XP_016865549.1:n.-355-104T=
XM_017010061.1:c.-459T= (MYOT) XP_016865550.1:n.-459T=
XM_017010062.1:c.-225+248T= (MYOT) XP_016865551.1:n.-225+248T=
XR_948815.2:n.347-11510A= (PKD2L2-DT)
NM_001135940.2:c.-197+248T= (MYOT) NP_001129412.1:n.-197+248T=
NM_001300911.2:c.-120-104T= (MYOT) NP_001287840.1:n.-120-104T=
NM_006790.3:c.122T= (MYOT) MANE Select NP_006781.1:p.Ile41=