Canonical Allele Identifier: CA446786376

Gene: MYOT PKD2L2-DT

Linked Data

• MyVariant Identifiers: chr5:g.137206553T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137870864T>G , CM000667.2:g.137870864T>G	GRCh38
NC_000005.9:g.137206553T>G , CM000667.1:g.137206553T>G	GRCh37
NC_000005.8:g.137234452T>G	NCBI36
NG_008894.1:g.8009T>G , LRG_201:g.8009T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239926.9:c.213T>G (MYOT) MANE Select	ENSP00000239926.4:p.Ala71=
ENST00000239926.8:c.213T>G (MYOT)	ENSP00000239926.4:p.Ala71=
ENST00000421631.6:c.-197+339T>G (MYOT)	ENSP00000391185.2:n.-197+339T>G
ENST00000509812.5:n.179+339T>G (MYOT)
ENST00000511625.5:n.179+339T>G (MYOT)
ENST00000515645.1:c.-120-13T>G (MYOT)	ENSP00000426281.1:n.-120-13T>G
NM_001135940.1:c.-197+339T>G (MYOT)	NP_001129412.1:n.-197+339T>G
NM_001300911.1:c.-120-13T>G (MYOT)	NP_001287840.1:n.-120-13T>G
NM_006790.2:c.213T>G , LRG_201t1:c.213T>G (MYOT)	NP_006781.1:p.Ala71=
XR_948815.1:n.220-11601A>C (PKD2L2-DT)
XR_948816.1:n.58-11601A>C (PKD2L2-DT)
XM_017010060.1:c.-355-13T>G (MYOT)	XP_016865549.1:n.-355-13T>G
XM_017010061.1:c.-368T>G (MYOT)	XP_016865550.1:n.-368T>G
XM_017010062.1:c.-225+339T>G (MYOT)	XP_016865551.1:n.-225+339T>G
XR_948815.2:n.347-11601A>C (PKD2L2-DT)
NM_001135940.2:c.-197+339T>G (MYOT)	NP_001129412.1:n.-197+339T>G
NM_001300911.2:c.-120-13T>G (MYOT)	NP_001287840.1:n.-120-13T>G
NM_006790.3:c.213T>G (MYOT) MANE Select	NP_006781.1:p.Ala71=