Canonical Allele Identifier: CA10259756
Gene: MEI1 HGNC NCBI

Linked Data

dbSNP Id: rs147348682

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.41699654T>G , CM000684.2:g.41699654T>G GRCh38
NC_000022.10:g.42095658T>G , CM000684.1:g.42095658T>G GRCh37
NC_000022.9:g.40425604T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000401548.8:c.116T>G MANE Select ENSP00000384115.3:p.Val39Gly
ENST00000401548.7:c.116T>G ENSP00000384115.3:p.Val39Gly
ENST00000540833.1:c.-665T>G ENSP00000444225.1:n.-665T>G
NM_152513.3:c.116T>G NP_689726.3:p.Val39Gly
XM_011529935.1:c.116T>G XP_011528237.1:p.Val39Gly
XM_011529936.1:c.116T>G XP_011528238.1:p.Val39Gly
XM_011529937.1:c.116T>G XP_011528239.1:p.Val39Gly
XM_011529938.1:c.116T>G XP_011528240.1:p.Val39Gly
XM_011529939.1:c.116T>G XP_011528241.1:p.Val39Gly
XM_011529940.1:c.116T>G XP_011528242.1:p.Val39Gly
XM_011529941.1:c.116T>G XP_011528243.1:p.Val39Gly
XM_011529943.1:c.116T>G XP_011528245.1:p.Val39Gly
XM_011529944.1:c.116T>G XP_011528246.1:p.Val39Gly
XM_011529945.1:c.116T>G XP_011528247.1:p.Val39Gly
XM_011529946.1:c.116T>G XP_011528248.1:p.Val39Gly
XM_011529947.1:c.116T>G XP_011528249.1:p.Val39Gly
XM_011529950.1:c.116T>G XP_011528252.1:p.Val39Gly
XM_011529951.1:c.116T>G XP_011528253.1:p.Val39Gly
XM_011529953.1:c.116T>G XP_011528255.1:p.Val39Gly
XM_011529955.1:c.116T>G XP_011528257.1:p.Val39Gly
XM_011529956.1:c.116T>G XP_011528258.1:p.Val39Gly
XR_937816.1:n.150T>G
XR_937817.1:n.150T>G
XR_937818.1:n.150T>G
XR_937819.1:n.150T>G
XR_937820.1:n.150T>G
XR_937821.1:n.150T>G
XR_937822.1:n.150T>G
XM_011529935.2:c.116T>G XP_011528237.1:p.Val39Gly
XM_011529936.2:c.116T>G XP_011528238.1:p.Val39Gly
XM_011529937.2:c.116T>G XP_011528239.1:p.Val39Gly
XM_011529938.2:c.116T>G XP_011528240.1:p.Val39Gly
XM_011529939.2:c.116T>G XP_011528241.1:p.Val39Gly
XM_011529940.2:c.116T>G XP_011528242.1:p.Val39Gly
XM_011529941.2:c.116T>G XP_011528243.1:p.Val39Gly
XM_011529943.2:c.116T>G XP_011528245.1:p.Val39Gly
XM_011529944.2:c.116T>G XP_011528246.1:p.Val39Gly
XM_011529945.3:c.116T>G XP_011528247.1:p.Val39Gly
XM_011529946.2:c.116T>G XP_011528248.1:p.Val39Gly
XM_011529947.2:c.116T>G XP_011528249.1:p.Val39Gly
XM_011529956.2:c.116T>G XP_011528258.1:p.Val39Gly
XM_017028633.2:c.116T>G XP_016884122.1:p.Val39Gly
XM_024452164.1:c.116T>G XP_024307932.1:p.Val39Gly
XR_001755172.2:n.150T>G
XR_001755173.2:n.150T>G
XR_001755174.1:n.150T>G
XR_937816.2:n.150T>G
XR_937817.2:n.150T>G
XR_937818.2:n.150T>G
XR_937821.2:n.150T>G
XR_937822.3:n.150T>G
NM_152513.4:c.116T>G MANE Select NP_689726.3:p.Val39Gly