Canonical Allele Identifier: CA12412649
Gene: C6orf10 HGNC NCBI

Linked Data

dbSNP Id: rs6910071

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32315077A>G , CM000668.2:g.32315077A>G GRCh38
NC_000006.11:g.32282854A>G , CM000668.1:g.32282854A>G GRCh37
NC_000006.10:g.32390832A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375007.8:c.574+7409T>C ENSP00000364146.4:p.=
ENST00000375015.8:c.577+1317T>C ENSP00000364155.4:p.=
ENST00000442822.6:c.553+695T>C ENSP00000411164.2:p.=
ENST00000447241.6:c.580+7409T>C ENSP00000415517.2:p.=
ENST00000527965.5:c.532+1317T>C ENSP00000435103.1:p.=
ENST00000533191.5:c.574+695T>C ENSP00000431199.1:p.=
ENST00000612031.4:c.580+695T>C ENSP00000480403.1:p.=
ENST00000617061.4:c.571+1317T>C ENSP00000482001.1:p.=
NM_001286474.1:c.574+695T>C NP_001273403.1:p.=
NM_001286475.1:c.532+1317T>C NP_001273404.1:p.=
NM_006781.4:c.580+7409T>C NP_006772.3:p.=
XM_011514235.1:c.578-407T>C XP_011512537.1:p.=
XM_011514236.1:c.578-407T>C XP_011512538.1:p.=
XM_011514237.1:c.613+7409T>C XP_011512539.1:p.=
XM_011514238.1:c.554-407T>C XP_011512540.1:p.=
XM_011514239.1:c.592+7409T>C XP_011512541.1:p.=
XM_011514240.1:c.580+7409T>C XP_011512542.1:p.=
XM_011514241.1:c.577+695T>C XP_011512543.1:p.=
XM_011514242.1:c.574+695T>C XP_011512544.1:p.=
XM_011514243.1:c.556+1317T>C XP_011512545.1:p.=
XM_011514244.1:c.553+695T>C XP_011512546.1:p.=
XM_011514245.1:c.535+7409T>C XP_011512547.1:p.=
XM_011514246.1:c.532+1317T>C XP_011512548.1:p.=
XM_011515039.1:c.422-50703A>G XP_011513341.1:p.=
XM_011515040.1:c.422-50703A>G XP_011513342.1:p.=
XM_017010182.1:c.242-407T>C XP_016865671.1:p.=
XM_017010183.1:c.314+695T>C XP_016865672.1:p.=
XM_024446306.1:c.338+695T>C XP_024302074.1:p.=
XM_024446307.1:c.656-407T>C XP_024302075.1:p.=
NM_001286474.2:c.574+695T>C NP_001273403.1:p.=
NM_001286475.2:c.532+1317T>C NP_001273404.1:p.=
NM_006781.5:c.580+7409T>C NP_006772.3:p.=