Canonical Allele Identifier: CA1585606865

Gene: MYOT PKD2L2-DT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137870699A= , CM000667.2:g.137870699A=	GRCh38
NC_000005.9:g.137206388A= , CM000667.1:g.137206388A=	GRCh37
NC_000005.8:g.137234287A=	NCBI36
NG_008894.1:g.7844A= , LRG_201:g.7844A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239926.9:c.48A= (MYOT) MANE Select	ENSP00000239926.4:p.Pro16=
ENST00000239926.8:c.48A= (MYOT)	ENSP00000239926.4:p.Pro16=
ENST00000421631.6:c.-197+174A= (MYOT)	ENSP00000391185.2:n.-197+174A=
ENST00000509812.5:n.179+174A= (MYOT)
ENST00000511625.5:n.179+174A= (MYOT)
ENST00000515645.1:c.-121+174A= (MYOT)	ENSP00000426281.1:n.-121+174A=
NM_001135940.1:c.-197+174A= (MYOT)	NP_001129412.1:n.-197+174A=
NM_001300911.1:c.-121+174A= (MYOT)	NP_001287840.1:n.-121+174A=
NM_006790.2:c.48A= , LRG_201t1:c.48A= (MYOT)	NP_006781.1:p.Pro16=
XR_948815.1:n.220-11436T= (PKD2L2-DT)
XR_948816.1:n.58-11436T= (PKD2L2-DT)
XM_017010060.1:c.-356+174A= (MYOT)	XP_016865549.1:n.-356+174A=
XM_017010061.1:c.-533A= (MYOT)	XP_016865550.1:n.-533A=
XM_017010062.1:c.-225+174A= (MYOT)	XP_016865551.1:n.-225+174A=
XR_948815.2:n.347-11436T= (PKD2L2-DT)
NM_001135940.2:c.-197+174A= (MYOT)	NP_001129412.1:n.-197+174A=
NM_001300911.2:c.-121+174A= (MYOT)	NP_001287840.1:n.-121+174A=
NM_006790.3:c.48A= (MYOT) MANE Select	NP_006781.1:p.Pro16=