Canonical Allele Identifier: CA446786424

Gene: MYOT PKD2L2-DT

Linked Data

• MyVariant Identifiers: chr5:g.137206628C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137870939C>T , CM000667.2:g.137870939C>T	GRCh38
NC_000005.9:g.137206628C>T , CM000667.1:g.137206628C>T	GRCh37
NC_000005.8:g.137234527C>T	NCBI36
NG_008894.1:g.8084C>T , LRG_201:g.8084C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000239926.9:c.288C>T (MYOT) MANE Select	ENSP00000239926.4:p.Phe96=
ENST00000239926.8:c.288C>T (MYOT)	ENSP00000239926.4:p.Phe96=
ENST00000421631.6:c.-197+414C>T (MYOT)	ENSP00000391185.2:n.-197+414C>T
ENST00000509812.5:n.179+414C>T (MYOT)
ENST00000511625.5:n.179+414C>T (MYOT)
ENST00000515645.1:c.-58C>T (MYOT)	ENSP00000426281.1:n.-58C>T
NM_001135940.1:c.-197+414C>T (MYOT)	NP_001129412.1:n.-197+414C>T
NM_001300911.1:c.-58C>T (MYOT)	NP_001287840.1:n.-58C>T
NM_006790.2:c.288C>T , LRG_201t1:c.288C>T (MYOT)	NP_006781.1:p.Phe96=
XR_948815.1:n.220-11676G>A (PKD2L2-DT)
XR_948816.1:n.58-11676G>A (PKD2L2-DT)
XM_017010060.1:c.-293C>T (MYOT)	XP_016865549.1:n.-293C>T
XM_017010061.1:c.-293C>T (MYOT)	XP_016865550.1:n.-293C>T
XM_017010062.1:c.-225+414C>T (MYOT)	XP_016865551.1:n.-225+414C>T
XR_948815.2:n.347-11676G>A (PKD2L2-DT)
NM_001135940.2:c.-197+414C>T (MYOT)	NP_001129412.1:n.-197+414C>T
NM_001300911.2:c.-58C>T (MYOT)	NP_001287840.1:n.-58C>T
NM_006790.3:c.288C>T (MYOT) MANE Select	NP_006781.1:p.Phe96=