Canonical Allele Identifier: CA1585606969
Gene: MYOT HGNC NCBI
PKD2L2-DT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.137870928_137870941delinsCCAGCCAGCTTCCT , CM000667.2:g.137870928_137870941delinsCCAGCCAGCTTCCT GRCh38
NC_000005.9:g.137206617_137206630delinsCCAGCCAGCTTCCT , CM000667.1:g.137206617_137206630delinsCCAGCCAGCTTCCT GRCh37
NC_000005.8:g.137234516_137234529delinsCCAGCCAGCTTCCT NCBI36
NG_008894.1:g.8073_8086delinsCCAGCCAGCTTCCT , LRG_201:g.8073_8086delinsCCAGCCAGCTTCCT

Transcript Alleles

HGVS Amino-acid change
ENST00000239926.9:c.277_290delinsCCAGCCAGCTTCCT (MYOT) MANE Select ENSP00000239926.4:p.Pro93=
ENST00000239926.8:c.277_290delinsCCAGCCAGCTTCCT (MYOT) ENSP00000239926.4:p.Pro93=
ENST00000421631.6:c.-197+403_-197+416delinsCCAGCCAGCTTCCT (MYOT) ENSP00000391185.2:n.-197+403_-197+416deli...
ENST00000509812.5:n.179+403_179+416delinsCCAGCCAGCTTCCT (MYOT)
ENST00000511625.5:n.179+403_179+416delinsCCAGCCAGCTTCCT (MYOT)
ENST00000515645.1:c.-69_-56delinsCCAGCCAGCTTCCT (MYOT) ENSP00000426281.1:n.-69_-56delinsCCAGCCAG...
NM_001135940.1:c.-197+403_-197+416delinsCCAGCCAGCTTCCT (MYOT) NP_001129412.1:n.-197+403_-197+416delinsC...
NM_001300911.1:c.-69_-56delinsCCAGCCAGCTTCCT (MYOT) NP_001287840.1:n.-69_-56delinsCCAGCCAGCTT...
NM_006790.2:c.277_290delinsCCAGCCAGCTTCCT , LRG_201t1:c.277_290delinsCCAGCCAGCTTCCT (MYOT) NP_006781.1:p.Pro93=
XR_948815.1:n.220-11678_220-11665delinsAGGAAGCTGGCTGG (PKD2L2-DT)
XR_948816.1:n.58-11678_58-11665delinsAGGAAGCTGGCTGG (PKD2L2-DT)
XM_017010060.1:c.-304_-291delinsCCAGCCAGCTTCCT (MYOT) XP_016865549.1:n.-304_-291delinsCCAGCCAGC...
XM_017010061.1:c.-304_-291delinsCCAGCCAGCTTCCT (MYOT) XP_016865550.1:n.-304_-291delinsCCAGCCAGC...
XM_017010062.1:c.-225+403_-225+416delinsCCAGCCAGCTTCCT (MYOT) XP_016865551.1:n.-225+403_-225+416delinsC...
XR_948815.2:n.347-11678_347-11665delinsAGGAAGCTGGCTGG (PKD2L2-DT)
NM_001135940.2:c.-197+403_-197+416delinsCCAGCCAGCTTCCT (MYOT) NP_001129412.1:n.-197+403_-197+416delinsC...
NM_001300911.2:c.-69_-56delinsCCAGCCAGCTTCCT (MYOT) NP_001287840.1:n.-69_-56delinsCCAGCCAGCTT...
NM_006790.3:c.277_290delinsCCAGCCAGCTTCCT (MYOT) MANE Select NP_006781.1:p.Pro93=