Canonical Allele Identifier: CA361054059

Gene: MYOT PKD2L2-DT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137875899C>T , CM000667.2:g.137875899C>T	GRCh38
NC_000005.9:g.137211588C>T , CM000667.1:g.137211588C>T	GRCh37
NC_000005.8:g.137239487C>T	NCBI36
NG_008894.1:g.13044C>T , LRG_201:g.13044C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006790.3:c.427C>T (MYOT) MANE Select	NP_006781.1:p.Pro143Ser
ENST00000239926.9:c.427C>T (MYOT) MANE Select	ENSP00000239926.4:p.Pro143Ser
NM_001135940.1:c.-126C>T (MYOT)	NP_001129412.1:n.-126C>T
NM_001135940.2:c.-126C>T (MYOT)	NP_001129412.1:n.-126C>T
NM_001300911.1:c.82C>T (MYOT)	NP_001287840.1:p.Pro28Ser
NM_001300911.2:c.82C>T (MYOT)	NP_001287840.1:p.Pro28Ser
NM_006790.2:c.427C>T , LRG_201t1:c.427C>T (MYOT)	NP_006781.1:p.Pro143Ser
ENST00000239926.8:c.427C>T (MYOT)	ENSP00000239926.4:p.Pro143Ser
ENST00000421631.6:c.-126C>T (MYOT)	ENSP00000391185.2:n.-126C>T
ENST00000509812.5:n.250C>T (MYOT)
ENST00000511625.5:n.250C>T (MYOT)
ENST00000515645.1:c.82C>T (MYOT)	ENSP00000426281.1:p.Pro28Ser
XM_017010060.1:c.-154C>T (MYOT)	XP_016865549.1:n.-154C>T
XM_017010061.1:c.-154C>T (MYOT)	XP_016865550.1:n.-154C>T
XM_017010062.1:c.-154C>T (MYOT)	XP_016865551.1:n.-154C>T
XR_948815.1:n.219+12261G>A (PKD2L2-DT)
XR_948815.2:n.346+12261G>A (PKD2L2-DT)
XR_948816.1:n.57+13248G>A (PKD2L2-DT)