Canonical Allele Identifier: CA1803237658
Gene: TMEM67 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.93808963A= , CM000670.2:g.93808963A= GRCh38
NC_000008.10:g.94821191A= , CM000670.1:g.94821191A= GRCh37
NC_000008.9:g.94890367A= NCBI36
NG_009190.1:g.59120A= , LRG_688:g.59120A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000323130.8:c.2556+7A= ENSP00000314488.4:n.2556+7A=
ENST00000409623.8:c.2511+7A= ENSP00000386966.4:n.2511+7A=
ENST00000452276.6:c.2439+7A= ENSP00000388671.2:n.2439+7A=
ENST00000453906.6:c.1674+7A= ENSP00000403035.2:n.1674+7A=
ENST00000518896.2:c.847+7A= ENSP00000507992.1:n.847+7A=
ENST00000520680.2:c.2679+7A= ENSP00000428785.2:n.2679+7A=
ENST00000521517.6:c.2457+7A= ENSP00000430740.2:n.2457+7A=
ENST00000681998.1:c.2377+7A= ENSP00000506773.1:n.2377+7A=
ENST00000682036.1:c.1797+7A= ENSP00000508390.1:n.1797+7A=
ENST00000682577.1:c.2329+7A= ENSP00000506963.1:n.2329+7A=
ENST00000682624.1:c.*2130+7A= ENSP00000508343.1:n.*2130+7A=
ENST00000682700.1:c.2556+7A= ENSP00000507627.1:n.2556+7A=
ENST00000682744.1:n.2094+7A=
ENST00000682804.1:n.2379+7A=
ENST00000682837.1:c.2045+7A= ENSP00000507920.1:n.2045+7A=
ENST00000682935.1:n.4606+7A=
ENST00000682984.1:c.2217+7A= ENSP00000507209.1:n.2217+7A=
ENST00000683078.1:c.2311+7A= ENSP00000506796.1:n.2311+7A=
ENST00000683223.1:c.2288+7A= ENSP00000507685.1:n.2288+7A=
ENST00000683238.1:n.3780+7A=
ENST00000683249.1:n.4153+7A=
ENST00000683336.1:c.2377+7A= ENSP00000507695.1:n.2377+7A=
ENST00000683362.1:c.2217+7A= ENSP00000506985.1:n.2217+7A=
ENST00000683850.1:n.2479+7A=
ENST00000683919.1:c.2486+7A= ENSP00000507617.1:n.2486+7A=
ENST00000683953.1:c.2467+7A= ENSP00000508375.1:n.2467+7A=
ENST00000684023.1:c.2533+7A= ENSP00000507461.1:n.2533+7A=
ENST00000684064.1:c.2247+7A= ENSP00000508192.1:n.2247+7A=
ENST00000684089.1:n.4106+7A=
ENST00000684149.1:c.*1735+7A= ENSP00000507943.1:n.*1735+7A=
ENST00000684343.1:c.753+7A= ENSP00000507591.1:n.753+7A=
ENST00000684416.1:n.2515+7A=
ENST00000684540.1:c.2486+7A= ENSP00000507987.1:n.2486+7A=
ENST00000453321.8:c.2556+7A= MANE Select ENSP00000389998.3:n.2556+7A=
ENST00000323130.7:c.2526+7A= ENSP00000314488.3:n.2526+7A=
ENST00000409623.7:c.2313+7A= ENSP00000386966.3:n.2313+7A=
ENST00000453321.7:c.2556+7A= ENSP00000389998.3:n.2556+7A=
ENST00000474944.5:n.1694+7A=
ENST00000519845.5:n.1288+7A=
NM_001142301.1:c.2313+7A= , LRG_688t2:c.2313+7A= NP_001135773.1:n.2313+7A=
NM_153704.5:c.2556+7A= , LRG_688t1:c.2556+7A= NP_714915.3:n.2556+7A=
NR_024522.1:n.2627+7A=
XM_006716686.2:c.2253+7A= XP_006716749.1:n.2253+7A=
XM_006716687.2:c.1956+7A= XP_006716750.1:n.1956+7A=
XM_011517363.1:c.1674+7A= XP_011515665.1:n.1674+7A=
XR_428387.1:n.2614+7A=
XR_928360.1:n.2614+7A=
XR_928361.1:n.2614+7A=
XR_928362.1:n.2614+7A=
XM_006716686.4:c.2253+7A= XP_006716749.1:n.2253+7A=
XM_011517363.3:c.1674+7A= XP_011515665.1:n.1674+7A=
XM_024447326.1:c.1902+7A= XP_024303094.1:n.1902+7A=
XR_001745619.2:n.2597+7A=
XR_428387.2:n.2597+7A=
XR_928360.3:n.2597+7A=
XR_928362.3:n.2597+7A=
NM_153704.6:c.2556+7A= MANE Select NP_714915.3:n.2556+7A=
NR_024522.2:n.2577+7A=