Canonical Allele Identifier: CA7749427
Community Standard Title: NM_001385001.1(MCTP2):c.207C>T (p.Ser69=)
Gene: MCTP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.94298472C>T , CM000677.2:g.94298472C>T GRCh38
NC_000015.9:g.94841701C>T , CM000677.1:g.94841701C>T GRCh37
NC_000015.8:g.92642705C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001385001.1:c.207C>T MANE Select NP_001371930.1:p.Ser69=
ENST00000357742.10:c.207C>T MANE Select ENSP00000350377.4:p.Ser69=
NM_001159643.1:c.207C>T NP_001153115.1:p.Ser69=
NM_001159643.2:c.207C>T NP_001153115.1:p.Ser69=
NM_001385002.1:c.207C>T NP_001371931.1:p.Ser69=
NM_001385003.1:c.207C>T NP_001371932.1:p.Ser69=
NM_001385004.1:c.207C>T NP_001371933.1:p.Ser69=
NM_001385005.1:c.207C>T NP_001371934.1:p.Ser69=
NM_001385006.1:c.207C>T NP_001371935.1:p.Ser69=
NM_001385007.1:c.-134C>T NP_001371936.1:n.-134C>T
NM_001385008.1:c.207C>T NP_001371937.1:p.Ser69=
NM_001385009.1:c.-33-15810C>T NP_001371938.1:n.-33-15810C>T
NM_001385010.1:c.-33-15810C>T NP_001371939.1:n.-33-15810C>T
NM_001385011.1:c.-134C>T NP_001371940.1:n.-134C>T
NM_018349.3:c.207C>T NP_060819.3:p.Ser69=
NM_018349.4:c.207C>T NP_060819.3:p.Ser69=
NR_169526.1:n.376C>T
NR_169527.1:n.486C>T
NR_169528.1:n.376C>T
NR_169529.1:n.486C>T
NR_169530.1:n.486C>T
NR_169531.1:n.376C>T
NR_169532.1:n.717C>T
ENST00000357742.8:c.207C>T ENSP00000350377.4:p.Ser69=
ENST00000357742.9:c.207C>T ENSP00000350377.4:p.Ser69=
ENST00000451018.7:c.207C>T ENSP00000395109.3:p.Ser69=
ENST00000456504.5:c.207C>T ENSP00000388887.1:p.Ser69=
ENST00000543482.5:c.207C>T ENSP00000438521.1:p.Ser69=
ENST00000556363.5:n.479C>T
ENST00000561608.5:n.475C>T
XM_005254955.2:c.207C>T XP_005255012.1:p.Ser69=
XM_005254955.4:c.207C>T XP_005255012.1:p.Ser69=
XM_006720603.2:c.207C>T XP_006720666.1:p.Ser69=
XM_011521770.1:c.207C>T XP_011520072.1:p.Ser69=
XM_011521771.1:c.207C>T XP_011520073.1:p.Ser69=
XM_011521771.2:c.207C>T XP_011520073.1:p.Ser69=
XM_011521772.1:c.207C>T XP_011520074.1:p.Ser69=
XM_011521772.2:c.207C>T XP_011520074.1:p.Ser69=
XM_011521773.1:c.207C>T XP_011520075.1:p.Ser69=
XM_011521773.2:c.207C>T XP_011520075.1:p.Ser69=
XM_011521774.1:c.207C>T XP_011520076.1:p.Ser69=
XM_011521774.2:c.207C>T XP_011520076.1:p.Ser69=
XM_017022403.1:c.207C>T XP_016877892.1:p.Ser69=
XM_017022404.1:c.207C>T XP_016877893.1:p.Ser69=
XM_017022405.1:c.207C>T XP_016877894.1:p.Ser69=
XM_024449982.1:c.-134C>T XP_024305750.1:n.-134C>T
XR_001751349.2:n.272C>T
XR_931865.1:n.272C>T
XR_931865.2:n.272C>T